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 the agency’s own highest classification or reported deaths or serious injuries, 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.

Filters

Agency

Category

Minimum severity

Clear filters

27151–27175 of 90153

  • SevereNHTSA·22V032000·2022-01-26

    Pierce Fire Trucks Recalled for Fuel Tube Cracking and Leak Risk

    Pierce Manufacturing is recalling 2015-2021 Enforcer, Quantum, Velocity, and Arrow XT fire trucks because fuel tubes may crack and leak high-pressure fuel, increasing fire risk.

    Product
    PIERCE — PIERCE ENFORCER, QUANTUM, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0377-2022·2022-01-26

    SENNA Syrup unit-dose cups recalled for microbial contamination

    Lohxa, LLC is recalling SENNA Syrup (sennosides) 8.8 mg/5 mL unit-dose cups due to microbial contamination of the non-sterile product. The recall affects Lot #AM1115S with expiration date 01/2023, distributed nationwide.

    Product
    SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0505-2022·2022-01-26

    Haifa Smoked Turbot Fish Recalled for Listeria Contamination

    D & M Smoked Fish, Inc. is recalling Haifa Smoked Turbot Cold Smoked (8 oz) because it may be contaminated with Listeria monocytogenes. The product was distributed in New York and New Jersey.

    Product
    "Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z."
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0451-2022·2022-01-26

    Medtronic HawkOne Directional Atherectomy Device Recalled for Tip Damage

    Medtronic is recalling 28,094 units of its HawkOne directional atherectomy system due to reports of catheter tip damage and detachment that can cause blood clots in blood vessels.

    Product
    Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-S and H1-S-INT, Small Vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) Compatible guidewire. The HawkOne directional atherectomy system is intended for use in atherectomy of the peripheral vasculature.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V034000·2022-01-26

    Audi vehicles recalled for rear axle misalignment causing premature tire wear

    Certain 2019-2021 Audi vehicles are recalled for rear axle misalignment that may cause premature tire wear and increase crash risk. Dealers will inspect and adjust the alignment at no charge, replacing any worn tires as needed.

    Product
    AUDI — AUDI S5, A4 ALLROAD, S7, Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0514-2022·2022-01-26

    SonarMed AirWave Monitor Kit recall due to alarm and sensor detection failures

    Covidien is recalling 66 SonarMed AirWave Monitor Kits because the alarm may fail to sound and sensors may be incorrectly detected as disconnected, potentially causing the monitor to stop monitoring patients without alerting staff.

    Product
    SonarMed AirWave Monitor Kit (Monitor, Sensor Cable, Power Cord), Item Code AW-M0001. used with endotracheal tube (ETT)
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0501-2022·2022-01-26

    Draeger Fabius MRI Anesthesia Machines recalled due to misrouted oxygen hoses

    Draeger Medical recalls 26 Fabius MRI Anesthesia Machines due to incorrectly routed internal oxygen hoses. The misrouting can cause oxygen flow to deviate from set levels, risking inadequate patient oxygenation.

    Product
    Draeger Fabius MRI Anesthesia Machine, Catalog Number 8607300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V033000·2022-01-26

    2021 Toyota Venza Hybrid rear turn signal lighting system failure recall

    Toyota is recalling certain 2021 Venza Hybrid vehicles due to water intrusion in rear turn signal lights, which can cause electrical short circuits and lighting failure, increasing crash risk.

    Product
    TOYOTA — TOYOTA VENZA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0513-2022·2022-01-26

    Dental implant kits recalled for mislabeled implant dimensions

    Straumann USA LLC is recalling certain Neodent Easypack dental implant kits due to mislabeling where packaging does not match the implant dimensions inside. Affected units contain 3.5x8mm implants instead of the labeled 3.5x13mm size.

    Product
    Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22058·2022-01-26

    Eguana Technologies Evolve Home Energy Storage Systems Recalled for Fire Hazard

    Eguana Technologies is recalling about 245 Evolve Home Energy Storage Systems because the lithium-ion battery modules can overheat and pose a fire hazard. Consumers should contact the company immediately to schedule a free repair or battery replacement.

    Product
    Evolve Home Energy Storage Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22060·2022-01-26

    Geri-Care Over-the-Counter Drugs Recalled for Non-Child-Resistant Packaging

    Geri-Care Pharmaceuticals is recalling about 800 bottles of over-the-counter acetaminophen and aspirin tablets because the packaging is not child resistant, posing a poisoning risk to young children.

    Product
    Over-the-counter drugs
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0504-2022·2022-01-26

    Gentueri Viral Transport Medium Recalled Due to Turbidity and Discoloration

    Gentueri Inc is recalling 4,150 units of Gentueri Viral Transport Medium (VTM) nationwide due to visual turbidity and discoloration that may compromise diagnostic samples in transit.

    Product
    Gentueri Viral Transport Medium (VTM), Sterile, IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0503-2022·2022-01-26

    VITROS High Sample Diluent A Reagent Produces Lower Than Expected Results

    Ortho-Clinical Diagnostics is recalling VITROS High Sample Diluent A Reagent Pack Lot 2190 because it produces lower than expected TSH test results. The recall affects 1,416 units distributed worldwide.

    Product
    VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0500-2022·2022-01-26

    ImagePilot diagnostic imaging software versions 1.92 and 1.93 measurement error recall

    Konica Minolta's ImagePilot versions 1.92 and 1.93 software may provide incorrect measurement calculations if improper power sequences are used with AeroDR or Momentum Panel systems.

    Product
    ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on display monitors for medical diagnostics Product number: ADFR and ADJC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0508-2022·2022-01-26

    Nethili Pickle Recalled for Undeclared Anchovy Content

    Aroma Meats LLC is recalling Nethili Pickle products distributed in Oregon because the label fails to disclose that the product contains anchovy, a common food allergen.

    Product
    Nethili Pickle is packaged in clear plastic pouch and product is visible. Incomplete declaration of net weight only LB showing. No UPC. Product is imported from Jampani Foods of India. The label is read in parts: "***NETHILI PICKLE ***LB ***Jampani Pickles***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0510-2022·2022-01-26

    Voyager Rollator Walkers Recalled for Wheel Separation and Fall Risk

    Compass Health Brands is recalling 3,734 Voyager Rollator walkers due to cracking wheel spokes that may cause wheels to separate from the axle, potentially resulting in patient falls and injuries.

    Product
    Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx (RLEU10BL, RLEU10PK, RLEU10WT) RLEU10BL Voyager Rollator Cobalt Blue UPC: 815067078066; RLEU10PK Voyager Rollator Rose Gold UPC: 815067078073; RLEU10WT Voyager Rollator Ice Palace UPC: 815067078080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0511-2022·2022-01-26

    Microbiological Reference Products Recalled for Bacterial Contamination

    Microbiologics Inc is recalling KWIK-STIK and LYFO DISK microbiological reference products contaminated with Staphylococcus epidermidis. Fifty-nine kits were distributed to multiple U.S. states and countries.

    Product
    KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis derived from ATCC 36299.
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-0512-2022·2022-01-26

    Dental Implant Mislabeling: Neodent Easypack Helix GM Acqua Dimension Error

    Straumann USA LLC recalls Neodent Easypack Helix GM Acqua dental implants due to mislabeling. Implants have incorrect dimensions compared to carton labels, which could affect surgical planning and placement.

    Product
    Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental implant Item 138.089
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22057·2022-01-26

    Children's Nightgowns Recalled for Flammability Standard Violation

    AOSKERA is recalling approximately 1,000 children's nightgowns sold on Amazon.com from October 2020 through May 2021 because they fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0497-2022·2022-01-26

    Senior Living Nurse Call Systems Failing to Alarm Due to Memory Issue

    Stanley Security Solutions is recalling 11 Senior Living Arial Emergency and Nurse Call Systems because they fail to alarm due to increased memory consumption, potentially preventing nursing staff from responding to resident emergencies.

    Product
    Senior Living Arial Emergency and Nurse Call Systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0499-2022·2022-01-26

    FDA Recalls Sensis Cardiac Diagnostic Systems for Software Measurement Error

    Sensis cardiac diagnostic systems used in catheterization and electrophysiology procedures are recalled due to a software error (version VD12A) that can temporarily disable cardiac output measurement. No illnesses have been reported.

    Product
    1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3. Sensis Vibe Combo, material # 11007642; UDI: 04056869010205 The Sensis recording system is a diagnostic and administrative tool supporting hemodynamic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0508-2022·2022-01-26

    Cardinal Infant Heel Warmer recalled due to unapproved labeling changes

    Philips North America recalls Cardinal Infant Heel Warmers because labeling was changed without FDA approval. The devices cannot be sold or distributed without new FDA clearance.

    Product
    Cardinal Infant Heel Warmer, Reference # 989805617251 11470-010T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0502-2022·2022-01-26

    Blood Collection Tubes Recalled Due to Lithium Heparin Variation

    Greiner Bio-One is recalling 889,200 blood collection tubes (Lot #B21053QG) due to variation in lithium heparin that may cause blood clotting. The tubes were distributed to ten U.S. states.

    Product
    greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 456087P
    Category
    Medical Device
    Distribution
    10 states
  • HighNHTSA·22V029000·2022-01-25

    Forest River Recalls Transit Buses Due to Fire Risk from Relay Module

    Forest River is recalling specific 2021-2023 transit buses because a failed relay module can increase the risk of a fire. Dealers will install a wire jumper harness free of charge.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS, STARCRAFT BUS COMMUTE, SENATOR II HD, ALLSTAR XLT, ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V030000·2022-01-25

    2021 Harley-Davidson Motorcycles Instrument Cluster May Fail in Cold Weather

    Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON RH1250S, RA1250S, RA1250
    Category
    Vehicle
    Distribution
    Distributed nationwide