The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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6176–6200 of 113874

  • HighFDA (Devices)·Z-0234-2026·2025-10-29

    Prefilled saline flush syringes recalled over sodium chloride concentration shortfall

    Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.

    Product
    Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0240-2026·2025-10-29

    Veritor Connect software recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the BD Veritor Plus Analyzer to BD Synapsys.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0239-2026·2025-10-29

    Automated microbiology systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0296-2026·2025-10-29

    Maxicam gamma cameras recalled over risk of detector falling from mount

    GE HealthCare is recalling 37 Maxicam gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Maxicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0302-2026·2025-10-29

    Sopha Medical Vision cameras recalled over risk of detector falling

    GE HealthCare is recalling 205 Sopha Medical Vision gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Sopha Medical Vision (SMV) DSXi/DST-XLi,/ DST-XL/ DSTi; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0298-2026·2025-10-29

    Millenium Myosight gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 82 Millenium Myosight gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium Myosight; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0214-2026·2025-10-29

    Central monitoring stations recalled over reboot loop at specific network sizes

    GE HealthCare is recalling 2,306 Carescape Central Stations running software V3.0.5 because the system can enter a continuous reboot cycle, losing central monitoring of connected patients.

    Product
    GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03; Medical Display, cathode ray tube
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0036-2026·2025-10-29

    Ketorolac injection vials recalled after glass particulate found in product

    Aspiro Pharma is recalling Ketorolac Tromethamine Injection USP 60 mg/2 mL across several lots because of particulate matter identified as glass.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0211-2026·2025-10-29

    Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0140-2026·2025-10-29

    Shredded imitation crabmeat recalled over potential Clostridium botulinum from temperature abuse

    Ocean's Kitchen is recalling 496 cases of shredded imitation crabmeat for potential contamination with Clostridium botulinum due to a risk of temperature abuse during chilled storage at the firm.

    Product
    Oceans Kitchen IMITATION CRABMEAT SHREDDED Made From Wild Fish, Refrigerated, vacuum package. Net wt. per bag 2.5 lbs. UPC 1 90456 75654 2. These 2.5lb. bags are not for retail sales. Each master case contains 12/2.5lbs. bags. Net wt. per case: 30lbs. UPC 14972195756549. Oceans
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0208-2026·2025-10-29

    Silicone stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0115-2026·2025-10-29

    Tovala frozen raw shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Tovala branded frozen raw phosphate free shrimp in 5 oz bags because it may have been contaminated with Cesium-137.

    Product
    Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0233-2026·2025-10-29

    Oral thermometer probes recalled after being programmed with rectal configuration

    Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.

    Product
    Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0099-2026·2025-10-29

    Pecan caramel clusters recalled because they may contain undeclared cashews

    Abdallah Incorporated is recalling 744 units of Lunds & Byerly's Pecan Caramel Clusters because the product may contain undeclared cashews.

    Product
    Lunds & Byerly's Premium confections. Pecan Caramel Cluster Dipped in milk chocolate. Net Wt 2.5 oz (71g) UPC 0 72431-01294 5. Produced for Lunds & Byerlys, Edina, MN 55424.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0128-2026·2025-10-29

    Bulk mozzarella slabs recalled over possible stainless steel pieces in product

    Leprino Foods is recalling 5,453,442 lbs of bulk mozzarella slabs because of possible stainless steel pieces in the product.

    Product
    LMPS 1.5" BULK MOZZARELLA. 11" X 14" X 1.5 slabs, approximately 10 lbs. each. Approx. 1125 lbs. packaged in corrugated totes. Product Code 100003207. Refrigeration at 34-40F.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·H-0093-2026·2025-10-29

    Freeze-dried strawberries and creme recalled over potential metal in product

    Georgia Nut Co is recalling 76,121 cases of tru fru Strawberries + Creme Freeze-Dried Fresh because of the potential for metal in the product.

    Product
    tru fru Strawberries + Creme Freeze-Dried Fresh, retail pouch 3.4oz UPC 850048358249, 6 retail units per case
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0241-2026·2025-10-29

    Interventional fluoroscopy systems recalled over control board corrosion affecting imaging

    Philips is recalling 29 Zenition 50 interventional fluoroscopic X-ray systems because corrosion of the image intensifier television control board may cause loss of imaging or poor image quality.

    Product
    Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0206-2026·2025-10-29

    ENFit sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0106-2026·2025-10-29

    Coca-Cola Zero Sugar cans recalled over potential metal foreign material

    Coca-Cola Southwest Beverages is recalling 1,115 units of Coca-Cola Zero Sugar 12 oz cans in Texas over the potential presence of metal foreign material.

    Product
    Coca-Cola Zero Sugar 12oz Can -12 pack 49000042559 / FEB0226MAA Coca-Cola Zero Sugar 12oz Can -35 pack 49000058499 / FEB0226MAA
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0235-2026·2025-10-29

    Microbiology data systems recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2. COMPUTER OPTIPLEX EPICENTER SPARE, Catalog Number: 441421. 3. Generic NUC 2, Catalog Number: 445398. 4. Nuc 5i5 Os Image Bow 2.X, C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0098-2026·2025-10-29

    Whole grain brown ready rice recalled over possible stones in product

    Mars Foods US is recalling 315 cases of Ben's Original Ready Rice Whole Grain Brown because of the possible presence of stones in the product.

    Product
    Ben's Original Ready Rice Whole Grain Brown, 8.8oz., UPC 0 54800 42334 7. 12 retail units per wholesale case.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0116-2026·2025-10-29

    Frozen shrimp skewers recalled in expanded cesium 137 contamination action

    Southwind Foods is recalling Great American branded frozen raw shrimp skewers made under insanitary conditions in which the product may have been contaminated with Cesium-137.

    Product
    Great American branded Frozen raw shrimp skewer; 1lb bag UPC: 829944002716; 829944002372
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·H-0112-2026·2025-10-29

    Frozen cooked shrimp recalled across four brands over cesium 137 contamination

    Southwind Foods is recalling frozen cooked shrimp under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·H-0097-2026·2025-10-29

    Long grain white ready rice recalled over possible stones in product

    Mars Foods US is recalling 273 cases of Ben's Original Ready Rice Original Long Grain White because of the possible presence of stones in the product.

    Product
    Ben's Original Ready Rice Original Long Grain White, 8.8oz., UPC 0 54800 42333 0. 12 retail units per wholesale case
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0083-2026·2025-10-29

    Jumbo meatball subs recalled over metal shavings in mozzarella ingredient

    MG Foods is recalling 117 Jumbo Meat Ball Subs because the mozzarella cheese ingredient has the potential to be contaminated with metal shavings.

    Product
    Jumbo Meat Ball Sub; Net Weight: 8.9oz; Product Code: Fresh Thru 10-15-25, 10/16/2025, 10/20/2025 In clear plastic packaging with white sticker label
    Category
    Food
    Distribution
    2 states