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

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

13051–13075 of 89742

  • HighFDA (Devices)·Z-1834-2024·2024-05-22

    Reagent Test Strips for Urinalysis Recalled Due to Missing Leukocytes Pad

    Macherey Nagel urinalysis test strips are recalled due to a missing leukocytes test pad on some packages, potentially resulting in false negative results for urinary tract infections and renal inflammation. Affected lot: 65402.

    Product
    Reagent Test Strips for Blood, Urobilinogen, Bilirubin, Protein, Nitrite, Ketones, Ascorbic Acid, Glucose, pH, Specific Gravity and Leucocytes in Urine by the Dip and Read Technique.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1801-2024·2024-05-22

    Medtronic Cardioplegia Adapters recalled for potential unsealed sterile packaging

    Medtronic is recalling seven models of cardioplegia adapters due to potential unsealed sterile packaging, which could compromise equipment sterility in cardiac surgery. No illnesses have been reported.

    Product
    Medtronic Cardioplegia Adapters: a) DLP¿ 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model Number 25009, b) DLP¿ 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model Number 25010, c) DLP¿ 30.5 cm (12 in) Multiple Perfusion Set, Model Number 14003…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1825-2024·2024-05-22

    Sophysa Pressio Ventricular Intracranial Pressure Monitoring Kit Recall Due to CSF Leakage Risk

    Sophysa is recalling the Pressio Ventricular Intracranial Pressure Monitoring Kit due to manufacturing defects causing cerebrospinal fluid leakage from the catheter. Undetected leaks during implantation could result in infection risk to patients.

    Product
    The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit monitoring is intended for monitoring intracranial ventricular pressure with tunneling (PSO-VT) indicated for use in intraventricular pressure monitoring and cerebrospinal fluid drainage application.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1788-2024·2024-05-22

    Prosthetic knee recalled due to firmware defect causing device shutdown

    Ossur RHEO KNEE prosthetic units recalled due to firmware issues causing unintended warnings and device shutdown, which could result in patient falls.

    Product
    RKN130003, RHEO KNEE 3 YR WARRANTY, MD, CE, External lower limb prosthetic component
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1793-2024·2024-05-22

    Medtronic Arterial Cannulae Recalled Due to Unsealed Sterile Packaging

    Medtronic Perfusion Systems is recalling multiple arterial cannula models worldwide due to potential for unsealed sterile packing. Compromised packaging may allow contamination of devices intended for clinical use.

    Product
    Medtronic Arterial Cannulae packaged as: a) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020; b) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220; c) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020; d) DLP¿ Curved…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1792-2024·2024-05-22

    TriMed Threaded IM Nails Recalled Due to Out-of-Spec Driver-Socket Defect

    TriMed Threaded IM Nail 3.6mm implants are being recalled due to a driver-socket defect that could prevent proper nail pickup or torque application. The recall affects 120 units from lot QM23087 distributed nationwide.

    Product
    TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1809-2024·2024-05-22

    Karl Storz Laser Surgical Instruments Recalled Due to Sterilization Concerns

    Karl Storz laser surgical instruments lack validated sterilization procedures, creating infection risk after reprocessing. The FDA has recalled 85 units distributed nationwide and in Argentina.

    Product
    LASER Application Instrument, 23 cm, REF: 8694; LEUNIG-GREVERS LASER Application, REF: 461000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1237-2024·2024-05-22

    Organic Yogi Echinacea Immune Support Tea Recalled for Pesticide Residues

    East West Tea Company is recalling Organic Yogi Echinacea Immune Support tea bags nationwide due to pesticide residues detected above FDA action levels.

    Product
    Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 tea bag, 16 tea bags per pack, 4 packs per box. UPC on box: 0 76950 45010 3. CASE GTIN: 60076950450105. East West Tea Company, LLC Eugene, OR Yogi Echinacea Immune Support, Caffeine Herbal…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1805-2024·2024-05-22

    Medtronic Venous Cannulae Recalled for Unsealed Sterile Packaging

    Medtronic Perfusion Systems is recalling 17,221 units of venous cannulae due to potential for unsealed sterile packaging. The devices were distributed worldwide to healthcare facilities.

    Product
    Medtronic Venous Cannulae: a) DLP¿ 20 Fr. Malleable Single Stage Venous Cannula, Model Number 68120, b) DLP¿ 24 Fr. Malleable Single Stage Venous Cannula, Model Number 68124, c) DLP¿ 28 Fr. Malleable Single Stage Venous Cannula, Model Number 68128, d) DLP¿ 30 Fr.…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1803-2024·2024-05-22

    Medtronic Intracoronary Shunts recalled for potential unsealed sterile packaging

    Medtronic Intracoronary Shunts may have compromised sterile packaging, potentially allowing contamination. The FDA Class II recall affects 1,410 units distributed worldwide.

    Product
    Medtronic Intracoronary Shunts: a) ClearView¿ 1.00 mm Intracoronary Shunt, Model Numbers: 31100; b) ClearView¿ 1.25 mm Intracoronary Shunt, Model Numbers: 31125; c) ClearView¿ 2.00 mm Intracoronary Shunt, Model Numbers: 31200
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1802-2024·2024-05-22

    Medtronic Disposable Pressure Display Sets recalled for unsealed sterile packaging

    Medtronic Perfusion Systems recalls 1,624 Disposable Pressure Display Sets (Models 61000 and 62000) distributed worldwide due to potential for unsealed sterile packing. No illnesses or injuries have been reported.

    Product
    Medtronic Disposable Pressure Display Sets: a) DLP¿ 114.3 cm (45 in), Model Number 61000; b) DLP¿ 114.3 cm (45 in), Model Number 62000
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·24V358000·2024-05-21

    Kia Recalls 2022 Niro EV Vehicles Due to Battery Fire Risk

    Kia is recalling 2022 Niro EV vehicles because a high-voltage battery safety plug may overheat and melt, potentially causing a fire or loss of drive power.

    Product
    KIA — KIA NIRO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E038000·2024-05-21

    Cummins Recalls L9 Diesel Engines Due to Fuel Hose Separation Risk

    Cummins is recalling L9 diesel engines because remote fuel filter hoses may separate, causing fuel leaks, fire risks, or engine stalls.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V356000·2024-05-21

    Turtle Top Recalls 2024 Vehicles Due to Seat Recliner Defect

    Turtle Top is recalling 2024 Van Terra, Terra Transit, Odyssey, and Odyssey XL vehicles because the seat recliner mechanism may not engage, increasing injury risk in a crash.

    Product
    TURTLE TOP — TURTLE TOP TERRA TRANSIT, ODYSSEY, VAN TERRA, ODYSSEY XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V355000·2024-05-21

    Prime-Time Ford Transit Conversion Recall for Seat Recliner Defect

    Prime-Time is recalling 2023-2024 Ford Transit conversions because the seat recliner mechanism may not engage, increasing injury risk in a crash.

    Product
    PRIME-TIME — PRIME-TIME FORD TRANSIT CONVERSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V357000·2024-05-21

    Vermeer Recalls BC900XL Trailers Due to Incorrect Manual Torque Values

    Vermeer is recalling 2015-2022 BC900XL brush chipper trailers because the service manuals list incorrect lug nut torque values, which could lead to wheel detachment.

    Product
    VERMEER — VERMEER BC900XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V354000·2024-05-20

    ATC Recalls 2021-2024 Toy Hauler Trailers Due to Fire Risk

    ATC is recalling 2021-2024 Toy Hauler trailers because a faulty LED circuit board in the cooktop may overheat and cause a fire.

    Product
    ATC — ATC TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V353000·2024-05-20

    FR Conversions Recalls 2023-2024 Ram Promaster Vehicles for Seat Defect

    FR Conversions is recalling 2023-2024 Ram Promaster vehicles because the seat recliner mechanism may not engage, increasing injury risk during a crash.

    Product
    FR CONVERSIONS — FR CONVERSIONS RAM PROMASTER CONVERSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V352000·2024-05-17

    Braunability Recalls 2023-2024 Chrysler Wheelchair Vans for Seat Defect

    Braunability is recalling 2023-2024 Chrysler Voyager wheelchair vans because the seat recliner mechanism may not engage, increasing injury risk in a crash.

    Product
    BRAUNABILITY — BRAUNABILITY CHRYSLER WHEELCHAIR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V351000·2024-05-17

    2023–2025 Forest River Motorhomes Recalled for Unsecured LP Line

    Forest River is recalling certain 2023–2025 Solera, Forester, and Sunseeker motorhomes because the Liquid Propane line may not be properly secured, creating a fire risk if the line becomes damaged and leaks.

    Product
    FOREST RIVER — FOREST RIVER SUNSEEKER, SOLERA, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24235·2024-05-16

    Electrolux Frigidaire and Kenmore Electric Ranges Recalled for Fire and Burn Hazards

    Electrolux is recalling about 203,000 Frigidaire and Kenmore smooth-top electric ranges because heating elements can turn on unexpectedly, fail to turn off, or heat incorrectly, posing fire and burn risks. At least 212 incidents have been reported since 2009, including 14 fires and 8 burn injuries.

    Product
    Frigidaire and Kenmore Smooth-top Freestanding Electric Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V348000·2024-05-16

    2024 Lamborghini Urus Hood Latch May Separate While Driving

    Lamborghini is recalling 2023-2024 Urus Performante and Urus S vehicles because the hood latch striker may separate, causing the hood to open or detach while driving and create a road hazard.

    Product
    LAMBORGHINI — LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24236·2024-05-16

    CHZHVAN Combination Smoke and Carbon Monoxide Detectors Recalled for Failure to Alert

    CHZHVAN combination smoke and carbon monoxide detectors can fail to activate and may not alert users to a fire. About 6,800 units sold online via Amazon.com from August 2023 through January 2024 are affected.

    Product
    CHZHVAN Combination Smoke and Carbon Monoxide Detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide