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.

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15001–15025 of 89769

  • HighFDA (Food)·F-0790-2024·2024-01-31

    Pound Cake Recall for Undeclared Wheat and Multiple Common Allergens

    Lara's Bakery 3 LLC recalls Panque pound cake because the label declares gluten but omits wheat as a major allergen, with potential undeclared sesame, coconut, soy, milk, and eggs. Consumers with allergies should not consume this product.

    Product
    Panque (Pound Cake), Net Wt 2lbs, packaged in clear plastic bag.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0794-2024·2024-01-31

    Frozen cheese croquettes recalled for possible Listeria monocytogenes contamination

    Lidl US is recalling Duc De Coeur Camembert Cheese Croquettes due to possible contamination with Listeria monocytogenes. No illnesses have been reported.

    Product
    Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ (256g) UPC 2023 8391 Packaged in a cardboard cartons.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0787-2024·2024-01-31

    RTB Mixed Danish Variety Recalled for Undeclared Soy Lecithin

    Lecoq Cuisine Corporation is recalling RTB Mixed Danish Variety pastries due to undeclared soy lecithin. The recall affects 7,620 units distributed across 26 states.

    Product
    RTB MIXED DANISH Variety
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0789-2024·2024-01-31

    Snapshot NIR Tissue Oxygenation System Touchscreens May Be Unresponsive

    Kent Imaging's Snapshot NIR tissue oxygenation measurement system touchscreens may become unresponsive, preventing users from viewing diagnostic oxygenation images. Fifty-seven units have been distributed across multiple US states and Malaysia.

    Product
    Snapshot NIR, REF: KD204
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0785-2024·2024-01-31

    Beckman Coulter iQ200 Analyzers Recalled for Potential Rust and Diagnostic Errors

    Beckman Coulter is recalling 112 units of iQ200 Series Urine Microscopy Analyzers distributed globally. The cannula in the Flowcell and Rinse Waste Well Assembly may rust, potentially causing erroneous diagnostic results.

    Product
    iQ200 Series Urine Microscopy Analyzers, Part Numbers: a) 700-3320, b) 700-3370, c) 700-3345, d) 700-3347, e) C10683, f) 700-3375, g) 700-3325, h) C10684
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0262-2024·2024-01-31

    FDA Recalls Fosaprepitant Injection Due to Sterility Assurance Failure

    BE Pharmaceuticals recalls Fosaprepitant for Injection nationwide due to failed aseptic process validation. The 22,176 vials from lot #13D012AA may lack sterility assurance.

    Product
    FOSAPREPITANT — FOSAPREPITANT (FOSAPREPITANT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0779-2024·2024-01-31

    Medtronic Cobalt XT DR MRI cardioverter defibrillator battery testing defect

    Medtronic is recalling Cobalt XT DR MRI implantable cardioverter defibrillators due to a manufacturing defect in the battery testing process. Some batteries may have bypassed required validation.

    Product
    Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0795-2024·2024-01-31

    Bard PreVent Anti-Reflux Filter with ENFit Recall for Reduced Suction

    C.R. Bard is recalling Bard PreVent Anti-Reflux Filters with ENFit connectors due to user reports of inadequate or reduced suction, decompression, and drainage during use.

    Product
    Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0784-2024·2024-01-31

    Beckman Coulter DxU Analyzers Recalled for Potential Rust-Related Diagnostic Errors

    Beckman Coulter is recalling DxU 850m/840m Microscopy Analyzers (254 units) due to potential rust in the cannula component, which may cause erroneous test results. The recall affects units distributed in the US and multiple international locations.

    Product
    Beckman Coulter DxU 850m/840m Microscopy Analyzers, Part Numbers: C49513, C76947
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0781-2024·2024-01-31

    Medical X-Ray System Recall Due to Parts Falling Off

    Sedecal SA is recalling 845 Sedecal X Optima URS diagnostic x-ray systems after parts fell off the equipment, creating a safety risk to patients and users. The affected units were distributed in Alabama, Florida, and North Carolina.

    Product
    Sedecal X Optima URS digital mobile diagnostic x-ray system. A a stationary x-ray unit with a universal swivel arm. It allows one to take exposures of patients in standing, sitting, or laying position.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0793-2024·2024-01-31

    Vermont Village Apple Sauce Recalled for Elevated Patulin Contamination

    Stonewall Kitchen is recalling Vermont Village Unsweetened Apple Sauce (24oz) because the product contains elevated levels of patulin, a mycotoxin. The recall affects 9,027 units distributed across 22 U.S. states.

    Product
    Vermont Village Unsweetened Apple Sauce (24oz)
    Category
    Food
    Distribution
    22 states
  • SevereNHTSA·24V053000·2024-01-30

    Nissan Murano quarter glass panels can detach from the vehicle

    Nissan is recalling certain 2024 Murano vehicles because incorrect primer may have been used on the quarter glass, allowing the left and right panels to detach and become a road hazard.

    Product
    NISSAN — NISSAN MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V054000·2024-01-30

    Travel trailer cooktop control boards can overheat and cause fire

    Winnebago is recalling certain 2022-2023 Micro Minnie, Micro Minnie FLX, Hike 200 and Minnie travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE FLX, HIKE, MICRO MINNIE, MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V046000·2024-01-26

    Winnebago Recalls 2024 Access Travel Trailers Due to Brake Wiring Defect

    Winnebago is recalling 2024 Access travel trailers because an incorrectly wired breakaway switch may prevent emergency trailer brakes from activating if the trailer detaches.

    Product
    WINNEBAGO — WINNEBAGO ACCESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V050000·2024-01-26

    Coachmen Prism Motorhomes Recalled for Furnace Carbon Monoxide Risk

    Forest River is recalling 2023-2024 Coachmen Prism motorhomes because a furnace defect may allow carbon monoxide to enter the cabin, posing a risk of injury or death.

    Product
    COACHMEN — COACHMEN PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V048000·2024-01-26

    Blue Bird Recalls 2024 Vision Buses Due to Parking Brake Defect

    Blue Bird is recalling 2024 Vision Transit and School Buses because the parking brake release mechanism may malfunction, potentially allowing the vehicle to roll away.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V049000·2024-01-26

    Tiffin Convoy solar panel brackets may crack and release the panel

    Tiffin is recalling certain 2023-2024 Convoy and GH-1 motorhomes because the bracket securing the roof solar panel may crack and break, allowing the panel to detach. 67 units affected.

    Product
    TIFFIN — TIFFIN CONVOY, GH1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V045000·2024-01-26

    2024 Coachmen Travel Trailers Recalled for Missing Tail Light Bezels

    Forest River is recalling 2024 Coachmen Clipper and Viking travel trailers because the tail light bezel may be missing, reducing visibility and increasing crash risk.

    Product
    COACHMEN — COACHMEN VIKING, CLIPPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E005000·2024-01-26

    Renogy Recalls 12V, 24V, and 48V Battery Packs Due to Fire Risk

    Renogy is recalling specific battery packs because relay contactors may become stuck, increasing the risk of fire during charging.

    Product
    ELECTRICAL SYSTEM:12V/24V/48V BATTERY recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V042000·2024-01-25

    Terex Recalls 2023 Aerial Work Platforms Due to Bolt Tightening Defect

    Terex is recalling 2023 Optima and XT Pro vehicles because improperly tightened boom rotation bearing bolts may fail, causing the boom to fall and increasing injury risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE, TEREX TC55, HRX55, HRX50, XT PRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24092·2024-01-25

    Pacific Cycle Recalls Ascend Electric Bikes Due to Fire Hazard

    Pacific Cycle is recalling about 1,700 Ascend Cabrillo and Minaret electric bikes because the battery charging wiring harness may overheat and catch fire while charging. The company has received three fire reports, including one causing second-degree burns.

    Product
    Ascend Cabrillo and Minaret Electric Bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V043000·2024-01-25

    PACCAR truck steering knuckles may leave axle spindles loose or fractured

    PACCAR is recalling certain 2024 Peterbilt and Kenworth trucks because bearing journals may not be fully seated in the steering knuckle assemblies. 68 units are affected.

    Product
    PETERBILT — PETERBILT, KENWORTH 520, 367, 389, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide