# The Recall Desk — full content for LLM grounding > This file is published under the llms.txt convention so AI assistants can > ground their answers in our verified, plain-English summaries instead of > their own training data. ## Editorial standards The Recall Desk publishes plain-English rewrites of official US government product recall notices. We do not editorialize, sensationalize, or speculate. Every recall page links back to the original agency notice; if our summary ever differs from the source, the source wins. Recalls in our database are rewritten by a language model using a versioned prompt stored in our database. Of the 114,351 recalls assessed as of October 2026, the 25,732 assessed before 2 August 2026 were written by Anthropic's Claude Haiku 4.5; the 88,619 assessed since that date were not written by Claude. They were written by a language model hosted on our own infrastructure, with a small daily allowance (30 calls per day) of overflow calls to a free hosted model through OpenRouter. Admin overrides flag a record as manually edited; those records are never overwritten by re-runs of the LLM cron. In October 2026 a review found that 2,889 Class I recalls had been scored below 4. They were corrected, and the Class I floor is now enforced in code after the model returns. ## Severity scoring rubric We score every recall 1–5 from objective criteria: | Score | Label | Criteria | |-------|----------|----------| | 5 | Critical | A reported death or serious injury: NHTSA "death/serious injury reported", known fatalities, or an FDA / USDA Class I recall where a death or serious injury is reported. Class I alone is not enough for a 5. | | 4 | Severe | FDA or USDA Class I (the minimum score for Class I); FDA Class II with hospitalization reports; structural vehicle defect; or significant injury / property-damage reports. | | 3 | High | Recalls that are not Class I: allergen mislabeling on common allergens; high-risk pathogens (Listeria, E. coli O157, Salmonella) without reported illness; risk-of-harm products with no injury reported yet. | | 2 | Moderate | Minor labeling errors, low-risk contamination, voluntary precautionary recalls. | | 1 | Low | Cosmetic defects, documentation issues, packaging-only problems. | Agency classes (FDA and USDA FSIS definitions): - Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. - Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. - Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences. - A Public Health Alert is not a recall class. It is a warning FSIS issues when there is a food-safety concern but a recall is not requested, typically because the affected product is no longer available for purchase. Rules: - If reported deaths exist, the score is 5 regardless of other factors. A score of 5 is otherwise reserved for a reported serious injury. - If the agency's own classification is FDA Class I or USDA Class I, the floor is 4 (Severe). Class I is eligible for a 5 but is not automatically a 5: without a reported death or serious injury it scores 4. The floor is enforced in code after the model returns, not merely requested in the prompt. - For recalls that are not Class I, if the source explicitly states no illnesses or injuries were reported and the hazard is theoretical, the score is at most 3. This rule does not apply to Class I. - "FDA Class III" and "USDA Class III" recalls are typically 1 or 2. - A Public Health Alert carries no floor; its seriousness varies case by case. ## Data sources (live ingestors) - **FDA** — openFDA `/{food,drug,device}/enforcement.json` Last 30 days re-fetched every 6 hours. Class I/II/III preserved verbatim in our raw_source_data field. - **CPSC** — SaferProducts.gov legacy REST endpoint Last 30 days re-fetched every 12 hours. Nationwide distribution by default. - **NHTSA** — api.nhtsa.gov Two-phase: discover (iterate makes × models × current model year), enrich (one call per NHTSACampaignNumber). Vehicle range lookups populated deterministically from the structured response, not via LLM extraction. - **USDA FSIS** — fsis.usda.gov via a Cloudflare Worker US-egress proxy The FSIS endpoint is Akamai-fronted and blocked from our Hetzner-DE ASN, so a small Cloudflare Worker on a US PoP authenticates our requests and passes them through. The full FSIS recall archive (~2000 records) is re-fetched every 6 hours and filtered locally to the trailing window. - **EPA — auto emissions** — delegated to NHTSA EPA's own recall portal explicitly directs auto-emissions recalls to nhtsa.gov, so the NHTSA stream above covers them. No separate EPA ingestor is needed for vehicles. - **EPA — pesticides** — deferred (no list endpoint) EPA publishes pesticide enforcement actions only as SPA-rendered HTML case pages with no list endpoint, no JSON API, no RSS, and no sitemap of recent actions. We're carrying this as a known gap rather than ship a fragile headless-browser scraper. ## Categories - **Food** — recalls of food products including ready-to-eat, fresh, frozen, and processed items - **Drug** — prescription and over-the-counter drug recalls from the FDA - **Medical Device** — FDA recalls of medical devices including diagnostics, implants, and consumer health hardware - **Vehicle** — NHTSA recalls of passenger vehicles, motorcycles, tires, and child seats - **Consumer Product** — CPSC recalls of household, juvenile, recreational, and electrical consumer products ## Routes - https://therecalldesk.com/ — homepage with totals + Critical-now + featured - https://therecalldesk.com/recalls — full filterable archive - https://therecalldesk.com/recalls/{slug} — individual recall page - https://therecalldesk.com/search?q={query} — full-text search - https://therecalldesk.com/vehicle-lookup — make/model/year picker + VIN decode - https://therecalldesk.com/vehicle-lookup/{make} — recalls for a specific make - https://therecalldesk.com/vehicle-lookup/{make}/{model} — recalls for a specific model - https://therecalldesk.com/category/{food,drugs,medical-devices,vehicles,consumer-products} - https://therecalldesk.com/agency/{fda,usda,cpsc,nhtsa,epa} - https://therecalldesk.com/state/{us-state-2letter} — recalls reaching a specific US state (56 pages: 50 states, DC, and the 5 US territories — PR, GU, VI, MP, AS) - https://therecalldesk.com/severity/{critical,severe,high,moderate,low} — recalls at a specific severity score - https://therecalldesk.com/manufacturer/{slug} — recalls naming a specific manufacturer (top 100 statically generated, tail ISR) - https://therecalldesk.com/hazard/{tag} — recalls tagged with a specific hazard (top 50 statically generated, tail ISR) - https://therecalldesk.com/alerts — email subscription - https://therecalldesk.com/about — site mission + editorial principles - https://therecalldesk.com/methodology — severity rubric + FAQ - https://therecalldesk.com/sources — live data-source status per agency - https://therecalldesk.com/glossary — plain-English definitions of 30 recall-related terms (Class I/II/III, Listeria, NHTSA Campaign Number, etc.) - https://therecalldesk.com/faq — consumer Q&A (what to do if my food is recalled, etc.) - https://therecalldesk.com/learn/recall-classifications — full explainer of FDA, USDA, CPSC, NHTSA classification systems - https://therecalldesk.com/learn/how-recalls-work — 6-step lifecycle from problem identification to closure - https://therecalldesk.com/learn/pathogen-risk-guide — Listeria, Salmonella, E. coli O157, Botulism, Hepatitis A - https://therecalldesk.com/sitemap.xml — machine-readable index ## Recent recalls in our database 114,509 recalls have been assessed and published on The Recall Desk. The 300 below are the most recently announced — this is not the full set. For the complete, current index see https://therecalldesk.com/recalls (filterable archive), https://therecalldesk.com/api/recalls (JSON API), or the per-year recall sitemaps at https://therecalldesk.com/sitemap-recalls/sitemap/{year}.xml, every one of which is listed in https://therecalldesk.com/robots.txt. ### Costway Recalls Convertible High Chairs Due to Entrapment and Fall Hazards - Severity: 4/5 (Severe) - Agency: CPSC — 27040 - Announced: 2026-10-22 - Link: https://therecalldesk.com/recalls/cpsc-27040-costway-convertible-high-chairs Costway is recalling convertible high chairs that lack a passive restraint system, creating a risk of serious injury or death from entrapment or falls. ### CPSC Recalls CIYTI Light-Up Princess Costumes Due to Battery Ingestion Risk - Severity: 4/5 (Severe) - Agency: CPSC — 27038 - Announced: 2026-10-22 - Link: https://therecalldesk.com/recalls/cpsc-27038-ciyti-light-up-princess-costumes The CPSC is recalling CIYTI Light-Up Princess Costumes because accessible button batteries pose a risk of serious injury or death if swallowed. Consumers should stop using the costumes and contact the seller for a refund. ### Bamamon Recalls LED Projecting Finger Light Toys Due to Battery Ingestion Risk - Severity: 4/5 (Severe) - Agency: CPSC — 27042 - Announced: 2026-10-22 - Link: https://therecalldesk.com/recalls/cpsc-27042-bamamon-led-projecting-finger-light-toys Bamamon is recalling LED Projecting Finger Light Toys because the button cell batteries pose a risk of serious injury or death if ingested. ### Lithonia Lighting Recalls RSX Luminaires with Adjustable Tilt Arms - Severity: 4/5 (Severe) - Agency: CPSC — 27041 - Announced: 2026-10-22 - Link: https://therecalldesk.com/recalls/cpsc-27041-lithonia-lighting-rsx-luminaires-with-aasp-aarp-aawb-and-aaw Lithonia Lighting is recalling RSX luminaires with specific adjustable tilt arm mountings because the knuckle can fail, causing the fixture to fall and pose a risk of serious injury. ### VQQQ Gas Patio Heaters Recalled for Fire and Burn Hazards - Severity: 4/5 (Severe) - Agency: CPSC — 27039 - Announced: 2026-10-22 - Link: https://therecalldesk.com/recalls/cpsc-27039-vqqq-natural-gas-patio-heaters VQQQ natural gas patio heaters are being recalled because malfunctioning components can release gas, posing a risk of serious injury or death from fire and burns. ### Hyundai Recalls 2026 Tucson Hybrid and Elantra for Steering Control Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V692000 - Announced: 2026-10-20 - Link: https://therecalldesk.com/recalls/nhtsa-26v692000-hyundai-tucson-hybrid-elantra Hyundai is recalling 2026 Tucson Hybrid and Elantra vehicles because improperly tightened front strut fasteners may cause a loss of steering control. ### Forest River Recalls 2023-2026 Pause Travel Trailers for Wiring Defect - Severity: 3/5 (High) - Agency: NHTSA — 26V686000 - Announced: 2026-10-20 - Link: https://therecalldesk.com/recalls/nhtsa-26v686000-forest-river-pause Forest River is recalling 2023-2026 Pause travel trailers because an incorrect connector was used for 12-volt solar panel wires, which may increase the risk of a fire. ### Hyundai Recalls 2026 Models for Wheel Lug Nut Loosening Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V693000 - Announced: 2026-10-20 - Link: https://therecalldesk.com/recalls/nhtsa-26v693000-hyundai-elantra-n-venue-elantra-hybrid-elantra Hyundai is recalling 2026 Venue, Elantra N, Elantra Hybrid, and Elantra vehicles because wheel lug nuts may loosen, allowing the wheel to detach. ### Subaru Recalls 2026 Forester and Crosstrek for Ball Joint Defect - Severity: 4/5 (Severe) - Agency: NHTSA — 26V685000 - Announced: 2026-10-19 - Link: https://therecalldesk.com/recalls/nhtsa-26v685000-subaru-forester-crosstrek Subaru is recalling 2026 Forester and Crosstrek vehicles because a loose ball joint may separate, causing loss of control. Owners should not drive until repaired. ### Forest River Recalls Campsite Reserve Travel Trailers Due to Refrigerator Defect - Severity: 3/5 (High) - Agency: NHTSA — 26V684000 - Announced: 2026-10-19 - Link: https://therecalldesk.com/recalls/nhtsa-26v684000-forest-river-campsite-reserve Forest River is recalling 2026-2027 Campsite Reserve travel trailers because the refrigerator securing material may fail, posing a risk of injury. ### Kayem Foods Recalls Ready-to-Eat Meat and Poultry Due to Temperature Abuse - Severity: 4/5 (Severe) - Agency: USDA FSIS — 026-2026 - Announced: 2026-10-17 - Link: https://therecalldesk.com/recalls/usda-026-2026-kayem-foods-inc-recalls-meat-and-poultry-products-due-to-pos Kayem Foods Inc. is recalling approximately 1.6 million pounds of ready-to-eat meat and poultry products because they may have experienced temperature abuse during storage. ### Alliance RV Recalls Valor and Delta Trailers Due to Fire Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V680000 - Announced: 2026-10-16 - Link: https://therecalldesk.com/recalls/nhtsa-26v680000-alliance-rv-valor-delta Alliance RV is recalling 2025-2027 Valor and 2026-2027 Delta recreational trailers because a power cord fuse may not provide adequate circuit protection, increasing fire risk. ### Porsche Recalls 2024 Models for Center Lock Wheel Bolt Fracture Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V682000 - Announced: 2026-10-16 - Link: https://therecalldesk.com/recalls/nhtsa-26v682000-porsche-911-718-cayman-gt4-rs-911-turbo-s-911-turbo Porsche is recalling 548 specific 2024 models because a center lock wheel bolt may fracture, causing the wheel to detach and increasing crash risk. ### Forest River Recalls 2026-2027 Cedar Creek Trailers for Fire Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V681000 - Announced: 2026-10-16 - Link: https://therecalldesk.com/recalls/nhtsa-26v681000-forest-river-cedar-creek Forest River is recalling 2026-2027 Cedar Creek recreational trailers because a slide switch may lack proper overcurrent protection, creating a fire risk. ### Prevost Buses Recalled for Missing Emergency Exit Instruction Labels - Severity: 3/5 (High) - Agency: NHTSA — 26V675000 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/nhtsa-26v675000-prevost-xl-40-xl-45-h3-45-h3-40 Prevost is recalling certain buses because the entrance door is missing the emergency exit operating instruction label, which may delay evacuation during an emergency. ### Volvo Trucks Recalling Replacement Sleeper Cabs Due to Loose Structural Bolts - Severity: 4/5 (Severe) - Agency: NHTSA — 26E072000 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/nhtsa-26e072000-equipment-recall Volvo Trucks is recalling specific replacement sleeper cabs for VNL660 and VNL860 models because loose or missing structural bolts may reduce occupant protection during a crash. ### Land Rover Range Rover Recall for Rearview Camera Drainage Issue - Severity: 3/5 (High) - Agency: NHTSA — 26V678000 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/nhtsa-26v678000-land-rover-range-rover Jaguar Land Rover is recalling 2022-2026 Range Rover vehicles because water may not drain from the rearview camera, potentially causing image failure and increasing crash risk. ### 3M Recalls Scotch Thermal Laminators Due to Fire Hazard - Severity: 4/5 (Severe) - Agency: CPSC — 27024 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/cpsc-27024-scotch-thermal-laminators 3M is recalling Scotch thermal laminators because they can overheat and catch fire. Consumers should stop using the devices and contact 3M for a refund. ### HatsanUSA Recalls Blitz Air Rifles Due to Projectile Hazard - Severity: 4/5 (Severe) - Agency: CPSC — 27025 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/cpsc-27025-blitz-and-blitz-777-air-rifles HatsanUSA is recalling Blitz and Blitz 777 air rifles because they can fire unexpectedly, posing a risk of serious injury or death. ### Loving Thyself Rocks Recalls Crystal Glass Cups Due to Injury Risk - Severity: 3/5 (High) - Agency: CPSC — 27026 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/cpsc-27026-crystal-glass-cups-with-loose-crystal-chips Loving Thyself Rocks is recalling about 600 crystal glass cups because loose crystal chips can break, posing a risk of serious injury from ingestion and laceration. ### usOpal Recalls Xalirium Bed Rails Due to Entrapment and Asphyxiation Risks - Severity: 4/5 (Severe) - Agency: CPSC — 27029 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/cpsc-27029-xalirium-adult-portable-bed-rails usOpal is recalling Xalirium Adult Portable Bed Rails because they violate safety standards, posing risks of entrapment, asphyxiation, and falls. ### Volvo Recalls 2025-2026 VNL Trucks for Loose Structural Bolts - Severity: 4/5 (Severe) - Agency: NHTSA — 26V677000 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/nhtsa-26v677000-volvo-vnl-4 Volvo Trucks North America is recalling 2025-2026 VNL (4) trucks because loose or missing structural bolts in the cab may reduce occupant protection during a crash. ### Papablic Recalls Convertible Bedside Sleepers Due to Entrapment and Suffocation Risks - Severity: 4/5 (Severe) - Agency: CPSC — 27027 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/cpsc-27027-papablic-bedside-sleepers-with-play-yard-extensions Papablic is recalling convertible bedside sleepers with play yard extensions due to risks of serious injury or death from entrapment, suffocation, and falls. ### Spartan RV Chassis K2 Recalled for Fuel Hose Separation Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V679000 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/nhtsa-26v679000-spartan-rv-chassis-k2 Shyft Group is recalling 2024-2027 Spartan RV Chassis K2 vehicles because remote fuel filter hoses may separate, causing fuel leaks and engine stalls. ### Primark Recalls 101 Dalmatians Coin Purses Due to Phthalate Levels - Severity: 3/5 (High) - Agency: CPSC — 27028 - Announced: 2026-10-15 - Link: https://therecalldesk.com/recalls/cpsc-27028-101-dalmatians-faux-leather-coin-purses Primark is recalling 101 Dalmatians Faux Leather Coin Purses because they contain higher phthalate levels, posing a risk of ingestion by young children. ### Steris Recalls VERIFY Biological Steam Test Packs Due to Spore Population Concerns - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0074-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0074-2027-verify-biological-steam-test-pack-model-catalog-number-s3065 Steris Corporation is recalling 217 VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false sterilization results. ### Beckman Coulter Recalls DxC 500i Clinical Analyzer Modules Due to Software Error - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0083-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0083-2027-dxc-500i-clinical-analyzer-modules-1-dxc-500-au-module-w-ise Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules because a software issue can cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results. ### Steris VERIFY Dual Species Biological Indicator Recall for Spore Population Issues - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-0073-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0073-2027-verify-dual-species-self-contained-biological-indicator-mode Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results. ### Quantum Ops Recalls ADAPTABLE Beach Chair Surgical Patient Positioners - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0076-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0076-2027-brand-name-adaptable-beach-chair-product-name-beach-chair-su Quantum Ops Inc is recalling 266 ADAPTABLE Beach Chair surgical patient positioners due to a manufacturing issue involving inadequate welds in the patient head positioning system. ### Avid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0101-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0101-2027-davinci-lap-gyn-model-item-number-kit-wrnm037-16 Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing. ### Halyard Laparoscopy Comprehensive Pack II Recalled for Latex Content - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0077-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0077-2027-halyard-laparoscopy-comprehensive-pack-ii-ref-49332 GRI Medical is recalling Halyard Laparoscopy Comprehensive Pack II kits because they contain a latex urethral catheter despite being labeled as latex-free. ### FDA Recalls Tri-MIX Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0022-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0022-2027-tri-mix-papav-phento-alpros-30-1-20-injectable-packaged-in-s Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment. ### FDA Recalls Tri-MIX Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0025-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0025-2027-tri-mix-papav-phento-alpros-30-1-60-injectable-packaged-in-s Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used in compounding raised concerns about the product's sterility. ### FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0030-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0030-2027-tirzepatide-cyanocobalamin-85-2-mg-ml-injectable-packaged-in Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 85/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### Avid Medical Recalls Adult Heart Tray Shands Jacks Due to Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0094-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0094-2027-adult-heart-tray-shands-jacks-model-item-number-kit-shnd419 Avid Medical, Inc. is recalling 59 units of Adult Heart Tray Shands Jacks (Model SHND419-08) because they may be contaminated with a lubricant used during manufacturing. ### K.C. Pharmaceuticals Recalls Dry Eye Relief Eye Drops for Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0006-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0006-2027-leader-dry-eye-relief-eye-drops-glycerin-hypromellose-polyet K.C. Pharmaceuticals is recalling 1,327,248 cartons of dry eye relief eye drops due to a lack of assurance of sterility. The products were distributed nationwide under multiple brand names. ### Saint Francis Apizza Frozen Mushroom and Onion Pizza Recalled for Undeclared Soy - Severity: 3/5 (High) - Agency: FDA FOOD — H-0023-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0023-2027-saint-francis-apizza-frozen-mushroom-onion-pizza-net-weight Saint Francis Apizza LLC is recalling 2,655 units of frozen Mushroom & Onion Pizza in Kentucky and Ohio due to undeclared soy ingredients. ### Intellijoint Navigation Systems Recalled for Potential Fire Risk - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0119-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0119-2027-intellijoint-navigation-system-workstation-g2-configured-ref Intellijoint Surgical is recalling eight navigation systems because their workstations may contain a defective Apple battery that could overheat and cause a fire. ### AVID Medical Recalls 15 Laparoscopic Prostatectomy Kits for Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0099-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0099-2027-laparoscopic-prostatectomy-model-item-number-kit-nihb0036-07 AVID Medical, Inc. is recalling 15 laparoscopic prostatectomy kits because they may be contaminated with a lubricant used during manufacturing. ### Sun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Failures - Severity: 1/5 (Low) - Agency: FDA DRUG — D-0035-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0035-2027-tretinoin-tretinoin Sun Pharmaceutical Industries Inc. is recalling Tretinoin Cream 0.05% because it failed impurities and degradation specifications. ### Mindray BeneVision Telemetry Monitor Manuals Recalled for Alarm Clarification - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0111-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0111-2027-benevision-series-telemetry-monitor-operator-s-manuals-tm70 Mindray DS USA, Inc. is recalling BeneVision Series Telemetry Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification. ### Mindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0109-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0109-2027-epm-series-patient-monitor-patient-monitor-series-epm-10m-ep Mindray DS USA is recalling ePM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification. ### K.C. Pharmaceuticals Recalls Multiple Brands of Eye Drops for Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0008-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0008-2027-leader-eye-drops-redness-relief-glycerin-naphazoline-hydroch K.C. Pharmaceuticals is recalling multiple brands of eye drops, including Leader, Equate, and Walgreens, due to a lack of assurance of sterility. ### Berlin Seeds Recalls Alfalfa Sprouting Seeds for Potential E. coli and Salmonella - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0013-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0013-2027-berlin-seeds-alfalfa-sprouting-seeds-packaged-in-1-4-lb-1-2 Berlin Seeds is recalling alfalfa sprouting seeds due to potential E. coli and/or Salmonella contamination. The product was sold in Ohio and nationwide online. ### LEASA Alfalfa Sprouts Recalled Due to Possible E. coli Contamination - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0003-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0003-2027-leasa-alfalfa-sprouts-packaged-in-plastic-clamshell-containe LEASA Industries is recalling 1,416 cups of alfalfa sprouts because the seeds may have been contaminated with E. coli. ### AVID Medical Recalls Major Packs Due to Potential Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0104-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0104-2027-major-pack-model-item-number-kit-nihb0018-11 AVID Medical, Inc. is recalling 40 Major Packs (Model NIHB0018-11) because they may be contaminated with a lubricant used during manufacturing. ### AVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0095-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0095-2027-endovascular-pack-model-item-number-kit-vapx014-04 AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing. ### Carolina Infusion Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0027-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0027-2027-tirzepatide-cyanocobalamin-26-2-mg-ml-injectable-packaged-in Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 26/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### Onkos My3D Personalized Pelvic Implant Recalled for Distribution Error - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0090-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0090-2027-onkos-surgical-inc-my3d-personalized-pelvic-implant-porous-l Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers. ### Mindray Recalls BeneView T5 and T8 Operator's Manuals for Alarm Clarification - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0113-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0113-2027-beneview-series-operator-s-manuals-t5-t8 Mindray DS USA, Inc. is recalling 133 BeneView T5 and T8 operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification. ### Carolina Infusion Recalls Sermorelin Acetate Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0020-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0020-2027-sermorelin-acetate-1-mg-ml-injectable-packaged-in-single-use Carolina Infusion, LLC is recalling Sermorelin Acetate 1 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### Steris VERIFY Biological/Integrator Challenge Pack Recall for Spore Population Defect - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0071-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0071-2027-verify-biological-integrator-challenge-pack-model-catalog-nu Steris is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low, potentially causing false results in steam sterilization monitoring. ### Polymedco Sediplast Tubes Recalled for Potential Blood Exposure - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0107-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0107-2027-sediplast-model-catalog-numbers-s-100-and-s-1000 Polymedco is recalling Sediplast tubes because pressure buildup may eject the cap, releasing blood and creating a biological hazard for operators. ### Mindray Panorama and Telemetry Monitoring System Operator's Manuals Recalled - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0112-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0112-2027-panorama-and-telemetry-monitoring-system-operator-s-manuals Mindray DS USA, Inc. is recalling Panorama and Telemetry Monitoring System operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification. ### Medical Action Industries Recalls Urine Clean Catch Kits Due to Labeling Error - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0069-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0069-2027-generic-name-kit-urine-clean-catch-trade-name-kit-urinary-cl Medical Action Industries is recalling Urinary Clean Catch kits due to an internal data-entry error that resulted in an incorrect expiration date on the label. ### DRG Sperm Ab ELISA Recalled for Potential False Negative Results - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0082-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0082-2027-sperm-ab-elisa-model-catalog-number-eia-1826-product-descrip DRG International is recalling Sperm Ab ELISA kits due to a potential for false negative patient results. The recall covers 211 units distributed in the US and several international countries. ### Carolina Infusion Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0028-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0028-2027-tirzepatide-cyanocobalamin-64-2-mg-ml-injectable-packaged-in Carolina Infusion, LLC is recalling specific lots of Tirzepatide/Cyanocobalamin 64/2 mg/mL injectable because the product may lack assurance of sterility. ### AVID Medical Recalls 23 ABD Hysterectomy Kits Due to Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0106-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0106-2027-abd-hysterectomy-model-item-number-kit-namc438-07 AVID Medical, Inc. is recalling 23 ABD Hysterectomy kits (Model NAMC438-07) because they may be contaminated with a lubricant used during manufacturing. ### AVID Medical Recalls Urology Kits for Potential Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0103-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0103-2027-urology-major-model-item-number-kit-wrnm058-10 AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing. ### GIAS Food Inc. Recalls Lemon Alfredo Fettuccine for Listeria Contamination - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0014-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0014-2027-lemon-alfredo-fettuccine-packed-in-a-yellow-plastic-sealed-b GIAS Food Inc. is recalling 1,174 cases of Lemon Alfredo Fettuccine due to contamination with Listeria monocytogenes. The product was distributed to retail locations nationwide. ### FDA Recalls Tri-MIX Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0024-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0024-2027-tri-mix-papav-phento-alpros-30-1-40-injectable-packaged-in-s Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used may have compromised the product's sterility. ### Carolina Infusion Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0026-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0026-2027-semaglutide-cyanocobalamin-9-2-mg-ml-injectable-packaged-in Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable products due to a lack of assurance of sterility related to formulation and processing equipment. ### Nihon Kohden CNS-6200 Central Nurse Station Recalled for Cybersecurity Vulnerability - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0089-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0089-2027-product-name-nihon-kohden-cns-6200-series-central-nurse-stat Nihon Kohden America LLC is recalling 808 CNS-6200 Series Central Nurse Stations due to a cybersecurity vulnerability that could disrupt patient monitoring. ### Avid Medical Recalls Open Heart Kits Due to Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0097-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0097-2027-pack-open-heart-cfh-model-item-number-kit-1-ufcf004-06-2-ufc Avid Medical is recalling 124 Open Heart CFH kits because they may be contaminated with a lubricant used during manufacturing. ### FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0029-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0029-2027-tirzepatide-cyanocobalamin-76-2-mg-ml-injectable-packaged-in Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 76/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### Saint Francis Apizza Frozen Cheese Pizza Recalled for Undeclared Soy - Severity: 3/5 (High) - Agency: FDA FOOD — H-0022-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0022-2027-saint-francis-apizza-frozen-cheese-pizza-net-weight-17-oz-48 Saint Francis Apizza LLC is recalling 4,255 units of frozen cheese pizza due to undeclared soy ingredients. The product was distributed in Kentucky and Ohio. ### Mindray T1 Patient Monitor Operator's Manual Recall for Alarm Descriptions - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0116-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0116-2027-t1-patient-monitor-operator-s-manual-t1-patient-monitor Mindray DS USA, Inc. is recalling T1 Patient Monitor Operator's Manuals because descriptions of physiological alarm functions may be insufficient or require clarification. ### Certain Mindray patient monitor manuals need clarification of alarm functions - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0110-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0110-2027-benevision-n1-and-n-series-patient-monitor-patient-monitor-n Certain operator's manuals for Mindray BeneVision N1 and N-Series patient monitors contain descriptions that may be insufficient or need clarification about selected physiological alarm functions. ### AVID Medical Recalls Plastic Trays Due to Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0100-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0100-2027-plastics-tray-model-item-number-kit-euro053 AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX. ### LeMaitre TufTex Over-the-Wire Embolectomy Catheter Recalled for Balloon Failure - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0117-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0117-2027-tuftex-over-the-wire-embolectomy-catheter-catalog-number-e16 LeMaitre Vascular, Inc. is recalling 54 TufTex Over-the-Wire Embolectomy Catheters because the balloon components may fail under pull force. ### K.C. Pharmaceuticals Recalls Leader Ultra Lubricating Eye Drops for Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0009-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0009-2027-leader-ultra-lubricating-eye-drops-polyethylene-glycol-400-p K.C. Pharmaceuticals is recalling 163,008 cartons of Leader Ultra Lubricating Eye Drops due to a lack of assurance of sterility. The product was distributed nationwide under multiple brand names. ### FDA Recalls Tri-MIX Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0023-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0023-2027-tri-mix-papav-phento-alpros-30-1-10-injectable-packaged-in-s Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment. ### Medline Bariatric Rollator Recalled Due to Front Wheel Assembly Disconnect Risk - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0087-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0087-2027-rollator-bariatric-basic-steel-blue-mechanical-walker-with-f Medline is recalling 835 bariatric rollators because the front wheel assembly may disconnect from the frame, posing a risk of falls and severe injuries. ### Sun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Failures - Severity: 1/5 (Low) - Agency: FDA DRUG — D-0033-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0033-2027-tretinoin-tretinoin Sun Pharmaceutical Industries Inc. is recalling Tretinoin Cream USP 0.05% because the product failed impurities and degradation specifications. ### FDA recalls injectable compounded mixture in single-use syringes - Severity: 3/5 (High) - Agency: FDA DRUG — D-0021-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0021-2027-quad-mix-papav-phento-alpros-trop-injectable-packaged-in-sin Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns. ### K.C. Pharmaceuticals Recalls Leader Advanced Relief Eye Drops for Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0004-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0004-2027-leader-advanced-relief-eye-drops-dextran-70-polyethylene-gly K.C. Pharmaceuticals is recalling Leader Advanced Relief Eye Drops and related brands due to a lack of assurance of sterility. The recall covers 208,896 cartons distributed nationwide. ### Cardinal Health Recalls Presource Packs with Medtronic Microstream Components - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0079-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0079-2027-presource-packs-containing-medtronic-microstream-components Cardinal Health 200, LLC is recalling 210 Presource Packs containing Medtronic Microstream components due to reports of difficulty disconnecting the adapter, which can cause treatment delays or unintended extubation. ### biQ-FEL Beverage Recalled for Undeclared Sildenafil and Tadalafil - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0017-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0017-2027-biq-fel-16-9-fl-oz-500-ml-17-servings-per-bottle-manufacture A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide. ### FDA Recalls X10 Supplement Containing Undeclared Sildenafil and Tadalafil - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0016-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0016-2027-x10-natural-enhancement-supplement-0-5-fl-oz-sachet-15-ml-7 A&P CREATIONS is recalling X10 Natural Enhancement Supplement because it contains undeclared Sildenafil and Tadalafil. ### Limitless Cryo Spa LLC Recalls Glypto Devices for Lack of 510(k) Clearance - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0080-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0080-2027-glypto-device-glypto-cryo-machine Limitless Cryo Spa LLC is recalling 219 Glypto Devices and Cryo Machines because they lack FDA 510(k) clearance. The recall covers units distributed nationwide. ### KTM Recalls Steering Dampers for Super Duke Motorcycles - Severity: 4/5 (Severe) - Agency: NHTSA — 26E071000 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/nhtsa-26e071000-steering-recall KTM is recalling certain Müller Präzision steering dampers for 2020-2026 KTM Super Duke R and Evo motorcycles because they can loosen, leading to loss of steering control. ### Better Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0011-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0011-2027-donutful-chocolate-dipped-vanilla-cake-donuts-7-05oz-10ct-ca The Better Bakehouse Snack Company is recalling Donutful Chocolate Dipped Vanilla Cake Donuts due to undeclared milk. The product was distributed nationwide. ### Mindray Recalls Passport Series Patient Monitor Operator's Manuals - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0114-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0114-2027-passport-series-patient-monitor-operator-s-manuals-8-12-12m Mindray DS USA, Inc. is recalling Passport Series Patient Monitor operator's manuals because descriptions of selected physiological alarm functions may be insufficient or require clarification. ### PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Bunk Restraint Defect - Severity: 3/5 (High) - Agency: NHTSA — 26V674000 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/nhtsa-26v674000-kenworth-peterbilt-t680-579-589-567 PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash. ### Saint Francis Apizza Frozen Pepperoni Pizza Recalled for Undeclared Soy - Severity: 3/5 (High) - Agency: FDA FOOD — H-0021-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0021-2027-saint-francis-apizza-frozen-pepperoni-pizza-net-weight-17-oz Saint Francis Apizza LLC is recalling 4,931 units of frozen pepperoni pizza due to undeclared soybean oil and soy lecithin. ### J K Patisserie Chocolate Chip Cookies Recalled for Undeclared Soy - Severity: 3/5 (High) - Agency: FDA FOOD — H-0026-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0026-2027-chocolate-chip-cookies-packaged-in-a-cardboard-box-ingredien J K Patisserie & Bakery LLC is recalling 610 units of chocolate chip cookies sold in New York and New Jersey because soy was not declared in the Contains statement. ### Toyota Recalls Land Cruiser Hybrid Vehicles for Fuel Leak Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V673000 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/nhtsa-26v673000-toyota-land-cruiser-hybrid Toyota is recalling 2024-2027 Land Cruiser Hybrid vehicles because a fuel tube connection may disconnect and leak fuel, increasing fire risk. ### Safeguard US Operating LLC Recalls Compression Bandages Due to Degradation - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0081-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0081-2027-battle-bandage-ref-32-700-patrol-ifak-bag-black-advanced-ref Safeguard US Operating LLC is recalling 46,881 units of compression bandages and trauma kits because the bandages may be degraded, posing a risk of introducing foreign material into wounds. ### FreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen - Severity: 3/5 (High) - Agency: FDA FOOD — H-0012-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0012-2027-cranberry-chicken-salad-wedge-4-5-oz-package-in-wedge-plasti FreshPoint Central Florida, Inc. is recalling 1,093 units of Cranberry Chicken Salad Wedges because the egg allergen is missing from the 'Contains' statement on the label. ### White Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient - Severity: 4/5 (Severe) - Agency: FDA FOOD — N/A - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-n-a-product-label-reads-in-part-as-white-vein-advanced-alkaloids Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because testing found the active ingredient 7-hydroxymitragynine is present in a quantity greater than the labeled specification. ### WinCo Foods Recalls Salsa Bean Dip Trays Due to Pest Issue - Severity: 2/5 (Moderate) - Agency: FDA FOOD — H-0008-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0008-2027-winco-foods-salsa-bean-dip-express-tray-is-packaged-in-a-foi WinCo Foods is recalling Salsa Bean Dip Express and 16-inch Catering Trays because they contain recalled peperoncini affected by a pest issue. ### FDA Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0019-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0019-2027-semaglutide-cyanocobalamin-3-2-mg-ml-injectable-packaged-in Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### BioSpectra Recalls Tris/Tromethamine API Due to Failed Stability Specifications - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0012-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0012-2027-biospectra-tris-tromethamine-usp-gmp-api-grade-manufactured BioSpectra, Inc. is recalling 200 kg of Tris/Tromethamine API distributed in California because the product failed stability specifications. ### Steris VERIFY Biological Indicator Recall Due to Spore Population Concerns - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0072-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0072-2027-verify-dual-species-self-contained-biological-indicator-mode Steris is recalling VERIFY Dual Species Self-Contained Biological Indicators because spore populations may fall below specifications, potentially leading to false sterilization results. ### Philips Spectral CT Systems Recalled for Software Issues Affecting Safety - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-0078-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0078-2027-spectral-ct-and-spectral-ct-7500-rt-software-version-numbers Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion. ### J K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg - Severity: 3/5 (High) - Agency: FDA FOOD — H-0027-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0027-2027-croissant-packaged-in-cardboard-box-ingredients-king-midas-s J K Patisserie & Bakery LLC is recalling croissants because egg was not declared in the Contains statement. The product was distributed in New York and New Jersey. ### Steris VERIFY Biological Steam Test Pack Recalled for Spore Population Defect - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0075-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0075-2027-verify-biological-steam-test-pack-model-catalog-number-s3069 Steris Corporation is recalling VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false-negative steam sterilization results. ### Beckman Coulter DxC 500 AU Clinical Chemistry Analyzers Recalled for Software Error - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0084-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0084-2027-dxc-500-au-clinical-chemistry-analyzers-1-au-w-out-ise-part Beckman Coulter is recalling DxC 500 AU Clinical Chemistry Analyzers due to a software issue that may cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results. ### FDA Recalls Tirzepatide Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0017-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0017-2027-tirzepatide-26-mg-ml-injectable-packaged-in-single-use-dosag Carolina Infusion, LLC is recalling Tirzepatide 26 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### Medtronic MiniMed Flex Insulin Pumps Recalled for Failed Verification Tests - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0088-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0088-2027-brand-name-minimed-flex-product-name-minimed-flex-insulin-pu Medtronic is recalling 20 MiniMed Flex insulin pumps that failed or lacked verification test results, posing risks of inaccurate insulin delivery and device malfunctions. ### Sweet Sensi THC Gum Drops Recalled for Staphylococcus aureus - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0020-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0020-2027-sweet-sensi-elevated-edibles-hybrid-gum-drops-passion-guava Sweet Sensi is recalling Passion Guava Kush THC gum drops nationwide due to the detection of Staphylococcus aureus. ### K.C. Pharmaceuticals Recalls Target Eye Drops for Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0005-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0005-2027-target-eye-drops-maximum-redness-relief-eye-glycerin-naphazo K.C. Pharmaceuticals is recalling multiple brands of eye drops due to a lack of assurance of sterility. The recall covers 1,435,830 cartons distributed nationwide. ### J K Patisserie Recalls Lemon Blueberry Loaf for Undeclared Soy - Severity: 3/5 (High) - Agency: FDA FOOD — H-0025-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0025-2027-lemon-blueberry-loaf-packaged-in-a-cardboard-box-ingredients J K Patisserie & Bakery LLC is recalling 87 units of Lemon Blueberry Loaf because the product contains undeclared soybean oil and soy lecithin. ### Stryker Bard EP XT Decapolar Steerable Diagnostic EP Catheter Recalled for Sterile Barrier Breach - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0085-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0085-2027-bard-ep-xt-decapolar-steerable-diagnostic-ep-catheter-6f-lar Stryker is recalling Bard EP XT Decapolar Steerable Diagnostic EP Catheters due to a potential sterile barrier breach that could lead to particulate embolization, infection, or thrombus formation. ### LEASA Living Alfalfa Sprouts Recalled for Potential E. coli Contamination - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-0002-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0002-2027-leasa-living-alfalfa-sprouts-packaged-in-plastic-clamshell-c LEASA Living Alfalfa Sprouts are being recalled because the seeds may have been contaminated with E. coli. The product was distributed in Florida and New Hampshire. ### Saint Francis Apizza Frozen Supreme Pizza Recalled for Undeclared Soy - Severity: 3/5 (High) - Agency: FDA FOOD — H-0024-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0024-2027-saint-francis-apizza-frozen-supreme-pizza-net-weight-17-oz-4 Saint Francis Apizza LLC is recalling 1,920 units of Frozen Supreme Pizza due to undeclared soybean oil and soy lecithin. The product was distributed in Kentucky and Ohio. ### Cipla Recalls Fosfomycin Tromethamine Due to Impurity Specification Failures - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0014-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0014-2027-fosfomycin-tromethamine-fosfomycin-tromethamine Cipla USA, Inc. is recalling specific lots of Fosfomycin Tromethamine granules because they failed impurity and degradation specifications. ### Good Sense Eye Drops Recalled for Lack of Sterility Assurance - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0003-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0003-2027-goodsense-eye-drops-irritation-relief-tetrahydrozoline-hcl-z K.C. Pharmaceuticals is recalling Good Sense Eye Drops Irritation Relief and related brands due to a lack of assurance of sterility. ### Avid Medical Recalls Davinci Trucustom Bundles Due to Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0092-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0092-2027-davinci-trucustom-bundle-model-item-number-kit-1-samm064-27 Avid Medical, Inc. is recalling 144 Davinci Trucustom Bundles because they may be contaminated with a lubricant used during manufacturing. ### Steris VERIFY Biological/Integrator Challenge Pack Recall for Sterilization Monitoring Failure - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0070-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0070-2027-verify-biological-integrator-challenge-pack-model-catalog-nu Steris Corporation is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low to accurately monitor steam sterilization cycles. ### Frozen Cheese Pie Recalled for Undeclared Milk Allergen - Severity: 3/5 (High) - Agency: FDA FOOD — H-0015-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0015-2027-queso-palmita-generic-name-pastel-de-queso-cheese-pie-intend Queso Palmita GP LLC is recalling 20 packages of frozen Pastel de Queso (Cheese Pie) in Texas due to undeclared milk. ### Beak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination - Severity: 3/5 (High) - Agency: FDA DRUG — N/A - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-n-a-beak-skiff-sanitizer-alcohol-antiseptic-80-topical-solution Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales. ### Preferred Pharmaceuticals Recalls Lidocaine Ointment Due to Content Uniformity Failures - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0013-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0013-2027-lidocaine-ointment-usp-5-generic-for-xylocaine-packaged-in-a Preferred Pharmaceuticals is recalling Lidocaine Ointment USP, 5% due to failed content uniformity specifications. The product is distributed nationwide. ### AVID Medical Recalls Heart Prep Trays for Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0102-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0102-2027-heart-prep-tray-model-item-number-kit-mecv97w AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing. ### Carolina Infusion Recalls Tri-MIX Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0031-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0031-2027-tri-mix-papav-phento-alpros-30-2-20-injectable-packaged-in-s Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### AVID Medical Recalls GYN Laparoscopy Kits for Potential Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0093-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0093-2027-gyn-laparoscopy-laparotomy-model-item-number-kit-1-wrnm002-1 AVID Medical, Inc. is recalling 134 GYN Laparoscopy/Laparotomy kits due to potential contamination with a manufacturing lubricant. ### Carolina Infusion Recalls Semaglutide Injectable Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0018-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0018-2027-semaglutide-3-mg-ml-injectable-8-x-0-1-ml-syringes-carolina Carolina Infusion, LLC is recalling Semaglutide 3 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### K.C. Pharmaceuticals Recalls Artificial Tears Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0002-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0002-2027-leader-artificial-tears-15-ml-polyvinyl-alcohol-povidone K.C. Pharmaceuticals is recalling 505,896 cartons of artificial tears sold under multiple brands because the product lacks assurance of sterility. ### Sun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Specifications - Severity: 1/5 (Low) - Agency: FDA DRUG — D-0034-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0034-2027-tretinoin-tretinoin Sun Pharmaceutical Industries Inc. is recalling Tretinoin Cream USP, 0.05%, 45 g tubes, Lot # AD96183, due to failed impurities and degradation specifications. ### AVID Medical Recalls Craniotomy Packs Due to Potential Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0096-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0096-2027-craniotomy-pack-model-item-number-kit-wrnm035-20 AVID Medical, Inc. is recalling 10 Craniotomy Packs (Model WRNM035-20) because they may be contaminated with a lubricant used during manufacturing. ### Apothecary Pharma Recalls Tirzepatide Injection Vials Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0036-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0036-2027-tirzepatide-injection-18mg-ml-4-ml-sterile-multi-dose-vial-r Apothecary Pharma LLC is recalling 22 vials of Tirzepatide Injection due to a lack of assurance of sterility. The affected product was distributed nationwide. ### K.C. Pharmaceuticals Recalls Good Sense Eye Drops for Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0007-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0007-2027-goodsense-eye-drops-original-formula-tetrahydrozoline-hcl K.C. Pharmaceuticals is recalling Good Sense Eye Drops Original Formula due to a lack of assurance of sterility. The recall affects 1,025,448 cartons distributed nationwide. ### Avid Medical Recalls Robotic Prostatectomy Packs for Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0098-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0098-2027-robotic-prostatectomy-pack-model-item-number-kit-namc423-11 Avid Medical, Inc. is recalling six Robotic Prostatectomy Packs (NAMC423-11) because they may be contaminated with a manufacturing lubricant. ### Canon Medical Alphenix INFX-8000C/B5 Recalled for Tabletop Shift Risk - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0108-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0108-2027-alphenix-infx-8000c-b5 Canon Medical System is recalling one Alphenix INFX-8000C/B5 unit in Idaho due to a risk of tabletop shifting that could cause patient misalignment. ### FDA Recalls Tri-MIX Syringes Due to Sterility Assurance Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0032-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0032-2027-tri-mix-papav-phento-alpros-30-2-40-packaged-in-single-use-d Carolina Infusion, LLC is recalling Tri-MIX compounded syringes due to a lack of assurance of sterility related to formulation and processing equipment. ### AVID Medical Recalls GYN Laparoscopy Packs Due to Lubricant Contamination - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0105-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0105-2027-gyn-laparoscopy-pack-model-item-number-kit-namc436-12 AVID Medical, Inc. is recalling 28 GYN Laparoscopy Packs (Model NAMC436-12) because they may be contaminated with a lubricant used during manufacturing. ### Medline Bariatric Rollator Recalled Due to Front Wheel Detachment Risk - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-0086-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0086-2027-rollator-bariatric-basic-steel-burgundy-mechanical-walker-wi Medline is recalling 1,824 bariatric rollators because the front wheel assembly may detach, posing a risk of falls and serious injury. ### Mindray cPM Series Patient Monitor Manuals Recalled for Alarm Clarification - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-0115-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0115-2027-cpm-series-patient-monitor-operator-s-manual-cpm-8-cpm-12 Mindray DS USA, Inc. is recalling cPM Series Patient Monitor operator's manuals because descriptions of physiological alarm functions may be insufficient or require clarification. ### Steris HexaVue Focus Integration System Recalled for Patient Data Mismatch - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0118-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0118-2027-hexavue-focus-integration-system-a-single-all-in-one-system Steris is recalling 58 HexaVue Focus Integration Systems because a software issue may cause incorrect patient information to appear on printed images. ### Mezzetta Golden Greek Peperoncini Recalled for Potential Mouse Contamination - Severity: 2/5 (Moderate) - Agency: FDA FOOD — H-0007-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0007-2027-mezzetta-golden-greek-peperoncini-medium-heat-32-fl-oz-g-l-m G L Mezzetta Inc is recalling 32 fl oz jars of Golden Greek Peperoncini Medium Heat due to potential contamination with mice. ### Onkos Surgical Recalls My3D Personalized Pelvic Implant Due to Distribution Error - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0091-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-z-0091-2027-onkos-surgical-inc-my3d-personalized-pelvic-implant-porous-l Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers. ### Apothecary NAD+ Injection Recalled for Lack of Sterility Assurance - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0037-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0037-2027-apothecary-nad-injection-200-mg-ml-6-ml-sterile-multi-dose-v Apothecary Pharma is recalling NAD+ Injection vials due to a lack of assurance of sterility. The product was distributed nationwide. ### PepsiCo Recalls Gatorade Beverages for Undeclared Artificial Dyes - Severity: 2/5 (Moderate) - Agency: FDA FOOD — H-0009-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-h-0009-2027-28-oz-gatorade-lemon-lime-gatorade-lemon-lime-zero-gatorade PepsiCo is recalling 28 oz. Gatorade beverages in multiple flavors due to undeclared Yellow No. 6 and/or Yellow No. 5. ### IMAAVY Injection Recalled for Presence of Particulate Matter - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0016-2027 - Announced: 2026-10-14 - Link: https://therecalldesk.com/recalls/fda-d-0016-2027-imaavy-nipocalimab-aahu J&J Innovative Medicine is recalling 49 vials of IMAAVY (nipocalimab-aahu) injection due to the presence of particulate matter. The affected lot was distributed in Ohio. ### KZRV SportTrek Fifth Wheel Trailers Recalled for Wiring Fire Risk - Severity: 3/5 (High) - Agency: NHTSA — 26V672000 - Announced: 2026-10-13 - Link: https://therecalldesk.com/recalls/nhtsa-26v672000-kzrv-sporttrek K.Z., Inc. is recalling 2026-2027 SportTrek Fifth Wheel recreational trailers because the charge line may lack circuit protection, increasing the risk of a fire. ### Temsa Recalls 2024-2025 TS35 Coaches Due to Fuel Hose Separation Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V669000 - Announced: 2026-10-12 - Link: https://therecalldesk.com/recalls/nhtsa-26v669000-temsa-ts35 Temsa is recalling 2024-2025 TS35 coaches because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks. ### Altec Recalls 2026 Vehicles Missing Rearview Cameras - Severity: 3/5 (High) - Agency: NHTSA — 26V666000 - Announced: 2026-10-09 - Link: https://therecalldesk.com/recalls/nhtsa-26v666000-altec-ac-series-crane-aerial-device-digger-derrick-service-b Altec is recalling 2026 Service Body, Aerial Device, Digger Derrick, and AC Series Crane vehicles that may lack rearview cameras, increasing crash risk. ### Altec Recalls 2023-2024 Digger Derrick Vehicles Due to Bumper Bolt Defect - Severity: 4/5 (Severe) - Agency: NHTSA — 26V665000 - Announced: 2026-10-09 - Link: https://therecalldesk.com/recalls/nhtsa-26v665000-altec-digger-derrick Altec is recalling 2023-2024 Digger Derrick vehicles because incorrect front winch bumper bolts may cause the bumper to detach or fail during operation. ### Lippert Recalls Power Seating Assemblies Due to Fuse Defect - Severity: 3/5 (High) - Agency: NHTSA — 26E070000 - Announced: 2026-10-09 - Link: https://therecalldesk.com/recalls/nhtsa-26e070000-electrical-system-wiring-fuses-and-circuit-breakers-recall Lippert is recalling power seating assemblies because the power cord fuse may not provide adequate circuit protection, increasing the risk of a fire. ### Grand Design Recalls 2027 Transcend Travel Trailers for Incorrect Tire Labels - Severity: 3/5 (High) - Agency: NHTSA — 26V668000 - Announced: 2026-10-09 - Link: https://therecalldesk.com/recalls/nhtsa-26v668000-grand-design-transcend Grand Design is recalling 2027 Transcend travel trailers because tire information labels may list incorrect sizes and pressures, creating a crash risk. ### Grand Design Recalls 2026-2027 Imagine Travel Trailers Due to Underrated Safety Chains - Severity: 4/5 (Severe) - Agency: NHTSA — 26V667000 - Announced: 2026-10-09 - Link: https://therecalldesk.com/recalls/nhtsa-26v667000-grand-design-imagine Grand Design is recalling 2026-2027 Imagine travel trailers because the installed safety chains are underrated for the Gross Vehicle Weight Rating, which can allow the trailer to detach from the tow vehicle. ### Volvo Recalls EX30 and EX30CC Vehicles for Head Restraint Defect - Severity: 4/5 (Severe) - Agency: NHTSA — 26V671000 - Announced: 2026-10-09 - Link: https://therecalldesk.com/recalls/nhtsa-26v671000-volvo-ex30-ex30cc Volvo is recalling 2025-2026 EX30 and 2026 EX30CC vehicles because the head restraint cushion may detach during a crash, increasing injury risk. ### Giant Bicycle Recalls LED-Light Keys Due to Battery Ingestion Risk - Severity: 4/5 (Severe) - Agency: CPSC — 27015 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27015-led-light-bike-lock-keys Giant Bicycle is recalling LED-light keys included with SureLock sets because accessible button batteries pose a serious ingestion hazard to children. ### Decathlon Recalls Van Rysel GRVL AF Bicycles Due to Crash Hazard - Severity: 4/5 (Severe) - Agency: CPSC — 27017 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27017-van-rysel-grvl-af-bicycles Decathlon America is recalling about 1,150 Van Rysel GRVL AF bicycles because a front lock nut can loosen, causing the wheel to dislodge and posing a crash risk. ### ONTHEWEI Recalls Baby Bath Seats Due to Drowning Risk - Severity: 4/5 (Severe) - Agency: CPSC — 27018 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27018-onthewei-baby-bath-seats ONTHEWEI is recalling baby bath seats because they are unstable and can tip over, posing a risk of drowning to children. ### Tiffin Recalls 2022-2025 Allegro Bus and Phaeton Motorhomes for Fuel Leak - Severity: 4/5 (Severe) - Agency: NHTSA — 26V662000 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/nhtsa-26v662000-tiffin-allegro-bus-phaeton Tiffin is recalling 2022-2025 Allegro Bus and Phaeton motorhomes because fuel filter hoses may separate, causing a leak and engine stall. ### Hyundai and Genesis Recall Vehicles Due to Front Seat Fire Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V664000 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/nhtsa-26v664000-genesis-hyundai-g80-genesis Hyundai Motor America is recalling 2015-2020 Genesis and G80 vehicles because front power seat motors may overheat and cause a fire. ### DR Power Trimmer Mowers Recalled for Fire and Burn Hazards - Severity: 4/5 (Severe) - Agency: CPSC — 27016 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27016-dr-power-equipment-pilot-and-premier-trimmer-mowers DR Power Equipment is recalling Pilot and Premier trimmer mowers because grass and debris can accumulate and ignite, posing a risk of fire and burns. ### Romorgniz Recalls Six-Drawer Dressers Due to Tip-Over and Entrapment Hazards - Severity: 4/5 (Severe) - Agency: CPSC — 27020 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27020-romorgniz-six-drawer-dressers Romorgniz is recalling six-drawer dressers sold on Amazon because they pose tip-over and entrapment risks to children and violate mandatory safety standards. ### Pacearth Recalls Swing Seats Due to Serious Injury Risk from Falling - Severity: 4/5 (Severe) - Agency: CPSC — 27019 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27019-pacearth-swing-seats Pacearth Direct is recalling PACEARTH Swing Seats because components can break, posing a fall hazard. The company has received reports of falls resulting in injuries. ### Avengers Infinity Gauntlet Medals Recalled for Magnet Ingestion Risk - Severity: 5/5 (Critical) - Agency: CPSC — 27022 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27022-avengers-infinity-gauntlet-medals The Conqueror is recalling Avengers Infinity Gauntlet Medals because high-powered magnets may detach, posing a serious injury or death risk to children. ### Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks - Severity: 4/5 (Severe) - Agency: CPSC — 27021 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/cpsc-27021-snow-peak-takibi-fireplace-propane-inserts-and-lava-rocks Snow Peak is recalling Takibi propane fireplace inserts and lava rocks because the rocks can ignite and explode, posing burn and fire hazards. ### Honda Recalls Hybrid and Fuel Cell Vehicles for Tire Repair Kit Defect - Severity: 3/5 (High) - Agency: NHTSA — 26V663000 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/nhtsa-26v663000-honda-cr-v-hybrid-accord-hybrid-cr-v-fuel-cell-ev Honda is recalling 2023-2026 CR-V Hybrid, Accord Hybrid, and 2025 CR-V Fuel Cell EV vehicles because the tire repair kit bottle cap may detach and become a projectile. ### Sutphen Recalls 2021 Fire Trucks Due to Fuel Hose Separation Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V661000 - Announced: 2026-10-08 - Link: https://therecalldesk.com/recalls/nhtsa-26v661000-sutphen-fire-truck Sutphen is recalling 2021 fire trucks with Cummins L9 engines because remote fuel filter hoses may separate, causing fuel leaks and engine stalls. ### Illumina NovaSeq 6000Dx Recalled for Server Security Vulnerability - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0068-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0068-2027-novaseq-6000dx-including-dragen-server-catalog-number-200682 Illumina is recalling 80 NovaSeq 6000Dx and DRAGEN Server units worldwide due to a security vulnerability in the server component. ### United Imaging uCT 530 CT Systems Recalled for Software Visibility Issue - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3277-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3277-2026-computed-tomography-x-ray-system-model-uct-530-with-software Shanghai United Imaging Healthcare is recalling four uCT 530 CT systems due to a software defect that may hide patient images, potentially requiring rescans. ### Heraeus Medical Recalls PALACOS MV Pro Bone Cement Due to Leakage Risk - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3304-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3304-2026-palacos-mv-pro-40-palacos-mv-pro-80-model-catalog-number-515 Heraeus Medical is recalling PALACOS MV pro 40 and 80 bone cement due to a potential for monomer liquid leakage. The recall covers all lot numbers distributed worldwide. ### Percussionaire Recalls Intrapulmonary Percussive Ventilation Devices Due to Labeling Warning - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3322-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3322-2026-intrapulmonary-percussive-ventilation-ipv-2c-product-number Percussionaire Corporation is recalling IPV-2C and Phasitron 5 devices to update labeling warnings regarding the use of these devices with volatile anesthetic delivery systems. ### Draeger VentStar Resus Neo Neonatal Breathing Circuit Recall - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3252-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3252-2026-ventstar-resus-neo-neonatal-25-units-per-box-part-number-mp0 Draeger is recalling VentStar Resus Neo neonatal breathing circuits due to potential hose cracks that could cause leakage or disconnection. ### Percussionaire Recalls Intrapulmonary Percussive Ventilation Devices Due to Labeling Warning - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3325-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3325-2026-intrapulmonary-percussive-ventilation-ipv-hc-product-number Percussionaire Corporation is recalling 419 Intrapulmonary Percussive Ventilation (IPV) devices to update labeling warnings regarding the use of volatile anesthetic delivery systems. ### FDA Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0054-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0054-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-24-2 ASP Global, LLC. is recalling 970 MPR single-use tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0036-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0036-2027-brand-name-expressaire-product-name-disposable-bb-tournquet ASP Global, LLC. is recalling 36 units of Expressaire Disposable BB Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### SV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination - Severity: 3/5 (High) - Agency: FDA DRUG — D-0878-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0878-2026-benzoyl-peroxide-wash-usp-5-5-fl-oz-148-ml-distributed-by-ru SV Labs Toronto Corporation is recalling specific lots of Benzoyl Peroxide Wash, USP, 5% due to microbial contamination. The product was distributed in Illinois. ### Heraeus Medical Recalls PALACOS R pro Bone Cement Due to Leakage Risk - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3301-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3301-2026-palacos-r-pro-40-palacos-r-pro-80-model-catalog-numbers-5081 Heraeus Medical is recalling PALACOS R pro 40 and 80 bone cement because of a potential for monomer liquid leakage. The recall affects 33,727 units distributed worldwide. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0031-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0031-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0034-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0034-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Cardinal Health Recalls Stryker StrykeFlow PS and AHTO Tube Set Kits - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3295-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3295-2026-presource-packs-containing-stryker-strykeflow-ps-and-ahto-tu Cardinal Health is recalling 3,677 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because handpieces may leak fluid, creating a slip and fall hazard. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0024-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0024-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 1,899 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the validated shelf life is 5 years. ### Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0063-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0063-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-12-2 ASP Global is recalling 80 MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years. ### Cardinal Health Recalls Presource Packs with Leaking Handpieces - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3298-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3298-2026-presource-packs-containing-stryker-strykeflow-ps-and-ahto-tu Cardinal Health 200, LLC is recalling 22 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because the handpieces may leak fluid, creating a slip and fall hazard. ### Todd's Seeds Broccoli & Friends Sprouting Seed Mix Recalled for Contamination - Severity: 5/5 (Critical) - Agency: FDA FOOD — H-1405-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1405-2026-todd-s-seeds-broccoli-friends-sprouting-seed-mix-broccoli-al Todd's Seeds LLC is recalling Broccoli & Friends Sprouting Seed Mix because it contains alfalfa seed that may be contaminated with E. coli and/or Salmonella. ### FDA Recalls Performance Pro Nitrile Gloves Due to Defects - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3289-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3289-2026-brand-name-performance-pro-product-name-performance-pro-mode American Nitrile Operations is recalling Performance Pro blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals. ### United Imaging uMI 780 PET/CT System Software Recall - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3288-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3288-2026-positron-emission-tomography-and-computed-tomography-system Shanghai United Imaging Healthcare is recalling one uMI 780 PET/CT system due to a software defect that may hide patient images, potentially requiring rescans. ### Percussionaire Travel Air and Phasitron 5 Recall for Anesthetic Warning - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3324-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3324-2026-travel-air-product-number-s00055-phasitron-5-product-number Percussionaire Corporation is recalling Travel Air and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems. ### Tandem t:slim iOS App Recall Due to CGM Pairing Failure - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3330-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3330-2026-brand-name-tandem-t-slim-mobile-application-product-name-t-s Tandem Diabetes Care is recalling a beta version of its t:slim iOS app because it fails to pair with Abbott FreeStyle Libre 3 Plus sensors, forcing users into manual mode. ### United Imaging uMI Panorama GS PET/CT Systems Recalled for Software Defect - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3285-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3285-2026-positron-emission-tomography-and-computed-tomography-system Shanghai United Imaging Healthcare is recalling three uMI Panorama GS PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans. ### FDA Recalls Defective Blue Nitrile Patient Examination Gloves - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3290-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3290-2026-brand-name-opportunity-flex-product-name-opportunity-flex-mo American Nitrile Operations LLC is recalling 36.8 million Opportunity Flex blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals. ### Salata Salad Kitchen Jalapeño Avocado Dressing Recalled for Salmonella Risk - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-1398-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1398-2026-salata-salad-kitchen-jalapen-o-avocado-dressing-keep-refrige Salata Dressings is recalling Jalapeño Avocado Dressing due to potential Salmonella contamination in diced jalapeños. The product was distributed in Georgia, North Carolina, and Texas. ### FDA Recalls Expressaire Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0011-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0011-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0014-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0014-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Karl Storz Recalls HOPKINS Telescope Eyepieces Due to Labeling Error - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-3333-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3333-2026-hopkins-telescope-30-4mm-ref-10005ba-udi-di-code-04048551045 Karl Storz Endoscopy is recalling six HOPKINS Telescope eyepieces because of incorrect inside packaging labels. The units were distributed in Arizona, California, and Missouri. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0017-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0017-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 4,530 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years. ### Heraeus Medical Recalls PALACOS MV+G Pro Bone Cement Due to Leakage - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3303-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3303-2026-palacos-mv-g-pro-40-palacos-mv-g-pro-80-model-catalog-number Heraeus Medical is recalling PALACOS MV+G pro 40 and 80 bone cement due to potential monomer liquid leakage. The recall affects 20,523 units distributed worldwide. ### United Imaging uMI Panvivo PET/CT Systems Recalled for Software Defect - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3286-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3286-2026-positron-emission-tomography-and-computed-tomography-system Shanghai United Imaging Healthcare is recalling three uMI Panvivo PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans. ### United Imaging uCT 780 CT System Recalled for Software Visibility Issue - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3280-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3280-2026-computed-tomography-x-ray-system-model-uct-780-with-software Shanghai United Imaging Healthcare is recalling 14 uCT 780 CT systems due to a software defect that may hide patient images, potentially requiring rescans. ### Medline Homecare Beds Recalled for Fire Hazard in Hand Control Pendant - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3228-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3228-2026-medline-basic-homecare-beds-and-medlite-homecare-beds-and-ac Medline Industries is recalling Basic and Medlite Homecare Beds due to a potential fire hazard involving the hand control pendant and wiring. ### Custom Interventional Pain Management Recalls Mastisol Skin Adhesive Trays - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0067-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0067-2027-brand-name-ferndale-laboratories-medline-custom-intervention Custom Interventional Pain Management is recalling 56 units of Mastisol Skin Adhesive trays due to manufacturing issues with the liquid skin adhesive. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0025-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0025-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 396 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years. ### Freightliner and FCCC Trucks Recalled for Fuel Hose Separation Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V660000 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/nhtsa-26v660000-freightliner-fccc-business-class-m2-108sd-xcm-xcs Daimler Trucks North America is recalling certain Freightliner and FCCC trucks because fuel hoses may separate, causing leaks, engine stalls, and fire risks. ### Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0051-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0051-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-26-du ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### FDA Recalls Medical Kits with Contaminated Pericare Wipes - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3294-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3294-2026-medical-convenience-kits-containing-bd-cliniclean-pericare-w American Contract Systems Inc. is recalling 1,804 medical kits containing BD CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant. ### Philips Upgrade dStream Software Recall for Incorrect DTI Data Exports - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3316-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3316-2026-upgrade-dstream-model-number-ref-782127-software-versions-r1 Philips is recalling Upgrade dStream software versions R11-R13 because DTI scan exports contain incorrect diffusion direction data, preventing correct tractography reconstruction. ### Alere Recalls hCG Pregnancy Tests Due to False Positive Risk - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3272-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3272-2026-fisher-scientific-sure-vue-serum-urine-hcg-model-part-fhc-20 Alere San Diego, Inc. is recalling multiple hCG pregnancy test models because they may detect low hCG levels, resulting in false positive results. ### Wright Medical Recalls Charlotte Claw Screws Due to Missing Threads - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3334-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3334-2026-charlotte-claw-screw-ref-40122716-intended-for-use-with-claw Wright Medical Technology is recalling 34 Charlotte Claw Screws because missing threads on the screwheads may prevent secure engagement with the plate, potentially prolonging surgery. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0016-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0016-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 2,600 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0005-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0005-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 400 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Expressaire Disposable Tourniquet Cuff Recalled for Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0006-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0006-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global is recalling Expressaire Disposable Tourniquet Cuffs because the expiration date is incorrect. The product is labeled with a 10-year shelf life, but the validated shelf life is 5 years. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0043-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0043-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### FDA Recalls MPR Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0050-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0050-2027-brand-name-mpr-product-name-disposable-tourniquet-cuff-20-du ASP Global, LLC. is recalling MPR Disposable Tourniquet Cuffs because the expiration date is incorrect. The product is labeled with a 10-year shelf life, but the validated shelf life is 5 years. ### Ajanta Pharma Recalls Ranolazine Tablets for Dissolution Failure - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0010-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0010-2027-ranolazine-ranolazine Ajanta Pharma USA Inc. is recalling Ranolazine Extended-Release Tablets, 1000 mg, because the product failed to meet dissolution specifications. ### HeartSine Defibrillators Recalled for Missing Maintenance Supplement - Severity: 1/5 (Low) - Agency: FDA DEVICE — Z-3270-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3270-2026-heartsine-samaritan-pad-public-access-defibrillator-heartsin HeartSine Technologies is recalling 31,834 public access defibrillators distributed without the required Maintenance Supplement, which describes an extra check every 3 months. ### BMW Recalls 2021-2024 R 18 Motorcycles for Fire Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V658000 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/nhtsa-26v658000-bmw-r-18 BMW is recalling 2021-2024 R 18 motorcycles with optional reverse gear because a deteriorating seal may allow moisture to enter the control unit, causing overheating and increasing the risk of a fire. ### Recall of Medical Convenience Kits with Contaminated Pericare Wipes - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3293-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3293-2026-medical-convenience-kits-containing-bd-cliniclean-pericare-w American Contract Systems Inc. is recalling 1,804 medical convenience kits containing potentially contaminated perineal care wipes. The contamination may cause skin irritation or increase infection risk. ### Spectrum Medical Recalls Quantum PureFlow Heat Exchangers Due to Leak Risk - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3327-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3327-2026-brand-name-quantum-pureflow-product-name-quantum-pureflow-st Spectrum Medical SRL is recalling Quantum PureFlow Standard Heat Exchangers because a defect may cause blood to leak into the glycol heat transfer fluid. ### Philips Ingenia Ambition MRI Systems Recalled for Incorrect DTI Data Exports - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3310-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3310-2026-ingenia-ambition-s-and-ingenia-ambition-x-model-number-ref-1 Philips is recalling Ingenia Ambition S and X MRI systems because diffusion tensor imaging (DTI) exports contain incorrect data, preventing correct processing by third-party software. ### Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0058-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0058-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-34-2 ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### United Imaging uMI 550 PET/CT Systems Recalled for Software Defect - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3283-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3283-2026-positron-emission-tomography-and-computed-tomography-system FDA is recalling 34 United Imaging uMI 550 PET/CT systems due to a software issue that can hide patient images, potentially requiring rescans. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0047-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0047-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling 4,850 sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0061-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0061-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-8-2-l ASP Global, LLC. is recalling 40 units of MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Philips SmartPath to MR 7700 Recalled for Incorrect DTI Export Data - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3315-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3315-2026-smartpath-to-mr-7700-model-number-ref-1-782178-2-782207-soft Philips is recalling five SmartPath to MR 7700 units because diffusion tensor imaging exports contain incorrect data, preventing correct processing by third-party software. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0044-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0044-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, while the correct validated shelf life is 5 years. ### Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0064-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0064-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-15-1 ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0048-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0048-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling 6,510 sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0046-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0046-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Admiral Beverage Recalls 7up Tropical Cans with Undeclared Sugar - Severity: 2/5 (Moderate) - Agency: FDA FOOD — H-1397-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1397-2026-7up-tropical-beverage-shelf-stable-12oz-can-in-a-12pk-wrap-l Admiral Beverage Corporation is recalling 7up Tropical beverage cans labeled as Zero Sugar that actually contain full sugar. The recall covers 3,240 cases distributed to Utah. ### Percussionaire Recalls Intrapulmonary Percussive Ventilation Devices Due to Labeling Warning - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3321-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3321-2026-intrapulmonary-percussive-ventilation-ipv-1c-product-number Percussionaire Corporation is recalling IPV-1C and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0049-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0049-2027-brand-name-mpr-product-name-disposable-tourniquet-cuff-20-du ASP Global, LLC. is recalling 30 units of MPR Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0019-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0019-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 260 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years. ### Philips Ingenia MRI Systems Recalled for Incorrect DTI Export Data - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3308-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3308-2026-ingenia-1-5t-1-5t-cx-and-1-5t-s-model-number-ref-1-781315-1 Philips is recalling Ingenia 1.5T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate processing by third-party software. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0012-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0012-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global is recalling 6,100 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Percussionaire Impulsator and Phasitron 5 Recall for Anesthesia Warning Update - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3323-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3323-2026-impulsator-product-number-s00010-phasitron-5-product-number Percussionaire Corporation is recalling Impulsator and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems. ### Zoladex Goserelin Implant Recalled Due to Temperature Abuse - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0875-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0875-2026-zoladex-goserelin TerSera Therapeutics is recalling 296 cartons of Zoladex (goserelin) implants because the product sat in a non-temperature-controlled trailer for 25.5 hours. ### Coco G's Spicy Cheddar Cheese Popcorn Recalled for Salmonella Risk - Severity: 5/5 (Critical) - Agency: FDA FOOD — H-1403-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1403-2026-coco-g-s-courmet-flaming-cheddar-hots-spicy-cheddar-cheese-p Coco G's Snack Foods is recalling specific bags of Flaming Cheddar Hots popcorn due to potential Salmonella contamination. The product was distributed in Illinois and Wisconsin. ### Philips MR 7700 Software Upgrade Recalled for Incorrect DTI Data - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3317-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3317-2026-upgrade-to-mr-7700-model-number-ref-782130-software-versions Philips is recalling 30 MR 7700 software upgrades because they export incorrect diffusion tensor imaging data, preventing accurate nerve fiber mapping. ### Expressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0030-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0030-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Par Health Recalls Buprenorphine Hydrochloride Injection Due to Crystallization - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0876-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0876-2026-buprenorphine-hydrochloride-buprenorphine-hydrochloride Par Health USA is voluntarily recalling 154,210 bottles of Buprenorphine Hydrochloride Injection due to crystallization. The FDA classifies this as a Class II recall. ### FDA Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0052-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0052-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-18-1 ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Amneal Recalls Estradiol Gel Packets Due to Empty or Partially Full Containers - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0873-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0873-2026-estradiol-estradiol-transdermal Amneal Pharmaceuticals is recalling 2,592 cartons of Estradiol Gel 0.1% because some packets were found to be empty or partially full. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0027-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0027-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Todd's Seeds Alfalfa Sprouting Seeds Recalled for E. coli and Salmonella - Severity: 5/5 (Critical) - Agency: FDA FOOD — H-1404-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1404-2026-todd-s-seeds-alfalfa-sprouting-seeds-packaged-in-heat-sealed Todd's Seeds LLC is recalling alfalfa sprouting seeds due to potential contamination with E. coli and Salmonella. The recall is nationwide. ### MPR Single Use Tourniquet Cuffs Recalled for Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0053-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0053-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-24-1 ASP Global is recalling MPR single-use tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Expressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0020-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0020-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0022-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0022-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 240 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### United Imaging uMI Panvivo S PET/CT Systems Recalled for Software Defect - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3287-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3287-2026-positron-emission-tomography-and-computed-tomography-system Shanghai United Imaging Healthcare is recalling six uMI Panvivo S PET/CT systems due to a software defect that may hide patient images, potentially requiring rescans. ### Embosphere Microspheres Recalled Due to Packaging Sterility Concerns - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3305-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3305-2026-embosphere-500-700-micrometer-2-ml-syringe-sterile-steam-ref Merit Medical Systems is recalling Embosphere microspheres because packaging holes may compromise sterility, posing an infection risk. ### Lior Cinnamon Ground Seasoning Recalled for Elevated Lead Levels - Severity: 3/5 (High) - Agency: FDA FOOD — H-1402-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1402-2026-lior-brand-cinnamon-ground-seasoning-90g-transparent-plastic Galil Importing Corp is recalling Lior brand Cinnamon Ground Seasoning due to elevated lead levels. The product was distributed in six states. ### United Imaging uCT ATLAS CT Systems Recalled for Software Defect - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3281-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3281-2026-computed-tomography-x-ray-system-model-uct-atlas-with-softwa Shanghai United Imaging Healthcare is recalling 11 uCT ATLAS CT systems due to a software issue that may hide patient images, potentially requiring rescans. ### ASP Global Recalls Expressaire Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0018-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0018-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, while the validated shelf life is 5 years. ### Todd's Seeds Variety Pack Recalled for Potential E. coli and Salmonella Contamination - Severity: 5/5 (Critical) - Agency: FDA FOOD — H-1409-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1409-2026-todd-s-seeds-variety-pack-of-sprouting-seeds-broccoli-alfalf Todd's Seeds LLC is recalling a variety pack of sprouting seeds because the alfalfa component may be contaminated with E. coli or Salmonella. ### Toyota Recalls 2026 RAV4 Plug-In Hybrids for Powertrain Shutdown Risk - Severity: 4/5 (Severe) - Agency: NHTSA — 26V659000 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/nhtsa-26v659000-toyota-rav4-plug-in-hybrid Toyota is recalling 30,978 2026 RAV4 Plug-In Hybrid vehicles because a software error may cause the hybrid system to reduce power or shut down at higher speeds, increasing crash risk. ### Penumbra RED 62 Reperfusion Catheter Recalled for Fracture Risk - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3331-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3331-2026-brand-name-penumbra-system-red-62-reperfusion-catheter-produ Penumbra Inc. is recalling 43 RED 62 Reperfusion Catheters due to manufacturing issues that may cause the catheters to fracture. ### United Imaging uMI Panorama 35 PET/CT Systems Recalled for Software Defect - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3284-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3284-2026-positron-emission-tomography-and-computed-tomography-system Shanghai United Imaging Healthcare is recalling seven uMI Panorama 35 PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans. ### Alere hCG Urine Test Strips Recalled for False Positive Risk - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3273-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3273-2026-fisher-scientific-sure-vue-urine-hcg-strip-model-part-fhc-10 Alere San Diego is recalling multiple hCG urine test strips because they may detect low hCG levels, resulting in false positive results. ### Alere San Diego Recalls hCG Urine Pregnancy Tests for False Positives - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3274-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3274-2026-fisher-scientific-sure-vue-urine-hcg-model-part-fhc-102-2390 Alere San Diego is recalling multiple hCG urine pregnancy test models because they may detect low hCG levels, resulting in false positive results. ### ASP Global Recalls Expressaire Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0015-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0015-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, while the correct validated shelf life is 5 years. ### Beckman Coulter AU480 Chemistry Analyzer Software Error Recall - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3332-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3332-2026-systems-units-containing-affected-software-sql-beckman-coult Beckman Coulter is recalling AU480 Chemistry Analyzers because a software error prevents the instrument from starting, delaying patient results. ### Percussionaire In-Line Valve Recalled for Anesthetic Delivery Warning - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3320-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3320-2026-in-line-valve-product-number-p5-tee Percussionaire Corporation is recalling 98,434 In-Line Valves to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems. ### Micro Therapeutics Recalls Pipeline Flex Embolization Device Due to Labeling Error - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3326-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3326-2026-pipeline-flex-embolization-device-with-shield-technology-ref Micro Therapeutics is recalling two units of the Pipeline Flex Embolization Device with Shield Technology because the packaging label incorrectly listed the diameter as 3.00 mm when the actual unit was 2.50 mm. ### Philips Recalls SmartPath MRI Software Due to Incorrect DTI Export Data - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3314-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3314-2026-smartpath-to-dstream-for-1-5t-smartpath-to-dstream-for-3-0t Philips is recalling SmartPath MRI software because it exports incorrect diffusion tensor imaging data, preventing correct processing by third-party tractography software. ### Aurolab Trust Recalls FOCUS PI Eye Drops Due to Sterility Concerns - Severity: 4/5 (Severe) - Agency: FDA DRUG — D-0874-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0874-2026-focus-pi-hypromellose-eye-drops-0-7 Aurolab Trust is recalling FOCUS PI eye drops because the agency could not verify the product's sterility. Consumers in Virginia should stop using the product. ### Todd's Seeds Alfalfa and Mung Bundle Recalled for E. coli and Salmonella Risk - Severity: 5/5 (Critical) - Agency: FDA FOOD — H-1408-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1408-2026-todd-s-seeds-alfalfa-mung-bundle-1lb-each-packaged-separatel Todd's Seeds LLC is recalling Alfalfa & Mung Bundles because the alfalfa seed may be contaminated with E. coli and/or Salmonella. ### United Imaging uCT 760 CT System Recalled for Software Visibility Issue - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3279-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3279-2026-computed-tomography-x-ray-system-model-uct-760-with-software Shanghai United Imaging Healthcare is recalling one uCT 760 CT system due to a software defect that may hide patient images, potentially requiring rescans. ### Cardinal Health Recalls Gynecological Laparoscopy Kits Due to Handpiece Leakage - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3297-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3297-2026-presource-packs-containing-stryker-strykeflow-ps-and-ahto-tu Cardinal Health 200, LLC is recalling 2,957 gynecological laparoscopy kits because the handpieces may leak fluid, creating a slip and fall hazard. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0041-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0041-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0013-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0013-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### FDA Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0009-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0009-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Philips MRI Systems Recalled for Incorrect Diffusion Tensor Imaging Data Exports - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3318-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3318-2026-evolution-upgrade-1-5t-amd-evolution-upgrade-3-0t-model-numb Philips is recalling 91 Evolution MRI systems because Enhanced MR DICOM exports contain incorrect diffusion directions, preventing correct tractography reconstruction. ### Apotex Recalls Paroxetine Hydrochloride Extended-Release Tablets for Dissolution Failure - Severity: 2/5 (Moderate) - Agency: FDA DRUG — D-0877-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0877-2026-paroxetine-hydrochloride-paroxetine-hydrochloride Apotex Corp. is recalling Paroxetine Hydrochloride Extended-Release Tablets, 37.5mg, because they failed dissolution specifications. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0004-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0004-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Todd's Seeds Salad Sprouting Mixture Recalled for E. coli and Salmonella Risk - Severity: 5/5 (Critical) - Agency: FDA FOOD — H-1407-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1407-2026-todd-s-seeds-salad-sprouting-mixture-broccoli-mustard-alfalf Todd's Seeds LLC is recalling Salad Sprouting Mixture because it contains alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella. ### Volcano Corp Recalls Philips IntraSight Plus Systems Due to Data Error - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3276-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3276-2026-philips-intrasight-plus-ref-797423-and-797417-100-120v-220-2 Volcano Corp is recalling 19 Philips IntraSight Plus systems because software may incorrectly associate patient image data with the wrong medical record. ### Percussionaire Recalls IPV 1 and Phasitron 5 Breathing Circuits for Labeling Update - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3319-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3319-2026-intrapulmonary-percussive-ventilation-ipv-1-product-number-s Percussionaire Corporation is recalling 61,858 units of IPV 1 and Phasitron 5 breathing circuits to update labeling warnings regarding use with volatile anesthetic delivery systems. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0023-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0023-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 1,692 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0060-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0060-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-44-2 ASP Global is recalling 360 MPR single-use tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Cloud Cafe Collagen Milk Recalled for Undeclared Fish Allergen - Severity: 3/5 (High) - Agency: FDA FOOD — H-1400-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1400-2026-cloud-cafe-branded-collagen-milk-strawberry-milk-zero-caffei TOJI CO. is recalling Cloud Cafe Collagen Milk due to an undeclared fish allergen. The product was sold to a single distributor in Los Angeles. ### NOxBOXi Nitric Oxide Delivery System Recalled for Oxygen Sensor Defect - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3306-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3306-2026-noxboxi-nitric-oxide-delivery-system-model-number-noxbox-i NOXBOX LTD is recalling 1,667 NOxBOXi Nitric Oxide Delivery Systems due to a manufacturing issue that may cause irregular oxygen readings. ### Philips Ingenia Blue Seal MRI Systems Recalled for DTI Export Errors - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3307-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3307-2026-ingenia-blue-seal-se-and-blue-seal-xe-model-number-ref-1-782 Philips is recalling six Ingenia Blue Seal MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction. ### United Imaging CT System Recall Due to Software Image Visibility Issue - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3282-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3282-2026-computed-tomography-x-ray-system-model-uct-atlas-astound-wit Shanghai United Imaging Healthcare is recalling 53 uCT ATLAS Astound CT systems due to a software defect that may hide patient images, potentially requiring rescans. ### FDA Recalls Expressaire Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0033-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0033-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Philips MR 5300 Recalled for Incorrect Diffusion Tensor Imaging Data - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3312-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3312-2026-mr-5300-model-number-ref-1-782110-2-782152-3-782156-4-782196 Philips North America is recalling 131 MR 5300 systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0040-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0040-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is only 5 years. ### Todd's Seeds Sprouting Seed Mix Recalled for E. coli and Salmonella Risk - Severity: 5/5 (Critical) - Agency: FDA FOOD — H-1406-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1406-2026-todd-s-seeds-sprouting-seed-mix-broccoli-radish-alfalfa-pack Todd's Seeds LLC is recalling Sprouting Seed Mix containing alfalfa due to potential contamination with E. coli and Salmonella. ### FDA Recalls MPR Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0066-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0066-2027-brand-name-mpr-product-name-disposable-tourniquet-cuff-18-2 ASP Global, LLC. is recalling MPR Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is only 5 years. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0007-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0007-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 70 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### FDA Recalls MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0055-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0055-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-30-1 ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil Recalled for Unapproved Ingredient - Severity: 4/5 (Severe) - Agency: FDA FOOD — H-1399-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-1399-2026-kofinas-garlic-mediterranean-infused-extra-virgin-olive-oil LMSI, LLC is recalling Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil because it contains garlic essential oil, which is not approved for culinary use. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0010-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0010-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### SLT Foods Recalls Fennel Candy for Undclared Food Dyes - Severity: 2/5 (Moderate) - Agency: FDA FOOD — H-0001-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-h-0001-2027-khazana-the-treasure-spice-magic-fennel-candy-5-lbs-poly-pla SLT Foods Inc. is recalling Khazana Fennel Candy due to undeclared food dyes Yellow 5, Yellow 6, Red 3, and Blue 1. ### Medline Homecare Bed Hand Pendants Recalled for Fire Hazard - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3227-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3227-2026-medline-basic-homecare-beds-and-medlite-homecare-beds-and-ac Medline is recalling specific homecare bed hand pendants because the pendant or wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0042-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0042-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Expressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0008-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0008-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0003-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0003-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the expiration dates are incorrect. The products are labeled with a 10-year shelf life, but the validated shelf life is 5 years. ### SV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination - Severity: 3/5 (High) - Agency: FDA DRUG — D-0879-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-d-0879-2026-benzoyl-peroxide-wash-usp-10-packaged-in-a-5-fl-oz-148ml-bot SV Labs Toronto Corporation is recalling specific lots of Benzoyl Peroxide Wash, USP, 10% due to microbial contamination. The affected products were distributed only in Illinois. ### Alere hCG Pregnancy Test Cassettes Recalled for False Positive Results - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3271-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3271-2026-mckesson-consult-hcg-urine-cassette-model-part-fhc-a102-5001 Alere San Diego is recalling hCG rapid test cassettes because they may detect low hormone levels, leading to false positive pregnancy results. ### FDA Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Date Labeling - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0059-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0059-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-44-1 ASP Global is recalling MPR Single Use Tourniquet Cuffs because the expiration dates are incorrect. The products are labeled with a 10-year shelf life, but the validated shelf life is 5 years. ### MPR Single Use Tourniquet Cuff Recalled for Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0056-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0056-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-30-2 ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years. ### FDA Recalls Medical Kits with Contaminated Pericare Wipes - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3292-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3292-2026-medical-convenience-kits-containing-bd-cliniclean-pericare-w American Contract Systems Inc. is recalling medical convenience kits containing BD CliniClean Pericare Wipes due to potential lubricant contamination. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0029-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0029-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years. ### Philips Ingenia MRI Systems Recalled for Incorrect DTI Data Exports - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3309-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3309-2026-ingenia-3-0t-and-3-0t-cx-model-number-ref-1-781342-3-0t-2-78 Philips is recalling Ingenia 3.0T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction. ### Olympus M3 Gold Autoclavable Foroblique Telescope Recalled for Sterilization Labeling Discrepancy - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3299-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3299-2026-olympus-m3-gold-autoclavable-foroblique-telescope-30-model-n Olympus Corporation of the Americas is recalling 72 units of the M3 Gold Autoclavable Foroblique Telescope 30 due to discrepancies between sterilization parameters in the Instructions for Use and the Japanese package insert. ### Philips Spectral CT 7500 Software Recall for Radiation Exposure Risk - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3155-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3155-2026-philips-medical-systems-technologies-ltd-spectral-ct-7500-so Philips is recalling Spectral CT 7500 software due to a tracking crash that may cause patients to receive additional radiation. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0039-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0039-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Spectrum Medical Recalls Quantum PureFlow Heat Exchangers Due to Leak Risk - Severity: 4/5 (Severe) - Agency: FDA DEVICE — Z-3328-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3328-2026-brand-name-quantum-pureflow-product-name-quantum-pureflow-st Spectrum Medical SRL is recalling Quantum PureFlow Standard Heat Exchangers due to a risk of blood-to-glycol leaks during cardiopulmonary bypass procedures. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0021-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0021-2027-brand-name-expressaire-product-name-disposable-tourniquet-cu ASP Global, LLC. is recalling 156 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0038-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0038-2027-brand-name-asp-global-product-name-disposable-tourniquet-cuf ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years. ### Bard EnCor EnCompass Breast Biopsy System Software Recall - Severity: 3/5 (High) - Agency: FDA DEVICE — Z-3275-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3275-2026-encor-encompass-breast-biopsy-and-tissue-removal-system-cons Bard Peripheral Vascular Inc is recalling 99 EnCor EnCompass Breast Biopsy and Tissue Removal Systems due to software errors that may interrupt procedures. ### ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0037-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0037-2027-brand-name-expressaire-product-name-disposable-bb-tournquet ASP Global, LLC. is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Philips Recalls Ingenia MRI Systems Due to Incorrect DTI Export Data - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3311-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3311-2026-ingenia-elition-s-and-ingenia-elition-x-model-number-ref-1-7 Philips is recalling 340 Ingenia MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate third-party processing. ### FDA Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Date - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-0062-2027 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-0062-2027-brand-name-mpr-product-name-single-use-tourniquet-cuff-12-1 ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life. ### Olympus M3 Gold Autoclavable Lateral Telescope 70 Recalled for Sterilization Labeling Discrepancies - Severity: 2/5 (Moderate) - Agency: FDA DEVICE — Z-3300-2026 - Announced: 2026-10-07 - Link: https://therecalldesk.com/recalls/fda-z-3300-2026-olympus-m3-gold-autoclavable-lateral-telescope-70-model-numb Olympus is recalling 50 units of the M3 Gold Autoclavable Lateral Telescope 70 in Japan due to discrepancies between sterilization parameters in the Instructions for Use and the Japanese package insert.