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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13801–13825 of 27735

  • HighFDA (Drugs)·D-0355-2024·2024-03-06

    Omeprazole and Sodium Bicarbonate Prescription Drug Recalled Due to Subpotency

    Bausch Health Companies is recalling 3,600 cartons of Omeprazole and Sodium Bicarbonate nationwide. The drug was found to be subpotent, containing less active ingredient than specified.

    Product
    OMEPRAZOLE AND SODIUM BICARBONATE — OMEPRAZOLE AND SODIUM BICARBONATE (OMEPRAZOLE, SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1098-2024·2024-03-06

    MEDLINE Medical Device Kits Recalled for Potential Sterility Issues

    Medline Industries recalls multiple medical device kits and trays manufactured with components that may lack sterility. The affected solutions could be non-sterile, posing a potential safety risk.

    Product
    MEDLINE Kits, trays, and packs labeled as follows: a) Description, REF DYNDH1679; b) BREAST BIOPSY TRAY, REF DYNDH1664; c) BREAST BIOPSY TRAY, REF DYNDH1431A; d) BREAST BIOPSY TRAY, REF DYNJ46448; e) BREAST BIOPSY TRAY, REF DYKE1520B; f) COLON KIT- BERLIN, REF DYNDH1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0968-2024·2024-03-06

    Frito-Lay and Quaker Granola Bars Recalled for Potential Salmonella

    The Quaker Oats Co. recalled Frito-Lay Chips and Quaker Chewy Granola Bars variety packs due to potential Salmonella contamination. Products with best before date Aug-02-24 or earlier are affected.

    Product
    Frito-Lay Chips and Quaker Chewy Granola Bars Variety Pack; 40ct 36.94 oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0931-2024·2024-03-06

    Chin Jung White Kimchi Recalled Due to Undeclared Fish Allergen

    Chin Jung White Kimchi is being recalled because it contains undeclared fish, a common allergen. Consumers with fish allergies should not consume this product.

    Product
    Chin Jung White Kimchi - 3 lb. 8 oz (1.58 kg) plastic jars
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0998-2024·2024-03-06

    Munchies Snack Mix recalled due to potential Salmonella contamination

    The Quaker Oats Co. has recalled Munchies Snack Mix in the 0.875 oz 104 Count package due to potential Salmonella. The recall affects products with Best Before date of Aug-02-24 or earlier.

    Product
    Munchies Snack Mix (Munch Mix) 0.875 oz 104 Count
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0999-2024·2024-03-06

    Chewy candy snack recalled for potential Salmonella contamination

    Quaker Chewy Dipps Llama Rama snacks are being recalled nationally due to potential Salmonella contamination. Products with a Best Before date of Aug-02-24 or earlier are affected.

    Product
    Quaker Chewy Dipps Llama Rama 6ct 6.3oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0349-2024·2024-03-06

    FDA Recalls Fluticasone Propionate Nasal Spray Due to Suspected Bacterial Contamination

    The FDA is recalling Fluticasone Propionate Nasal Spray due to suspected potential presence of Burkholderia cepacia complex bacteria. The affected lot (TX5275) was distributed nationwide.

    Product
    FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0361-2024·2024-03-06

    Moxifloxacin Ophthalmic Injection Solution Recalled for Glass Particle Contamination

    Denver Solutions is recalling Moxifloxacin PF eye injection vials nationwide due to glass delamination in the vials. The affected product is used for eye surgery injections.

    Product
    Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1218-2024·2024-03-06

    Bone plates and surgical screws distributed without FDA pre-market clearance

    Acumed LLC is recalling 2,952,121 units of Acu-Loc bone plates, screws, and accessories distributed worldwide because they were placed on the market without FDA pre-market clearance. The safety and effectiveness of these devices have not been verified by the FDA.

    Product
    Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard, Left; 70-0045-S Acu-Loc VDU Plate Standard, Left; 70-0046 Acu-Loc VDU Plate Standard, Right; 70-0046-S Acu-Loc VDU Plate Standard, Right; 70-0047 Acu-Loc VDU Plate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1184-2024·2024-03-06

    Rebstock Holding Rod for Fixation May Move Uncontrollably

    The Rebstock Holding rod for fixation, a surgical instrument, may move or twist uncontrollably during use, potentially compromising patient safety if the movement transfers to attached equipment.

    Product
    Rebstock Holding rod for fixation -For holding and fixation of flexible Leyla Arms and spatula Art. No. 06-06-285 and 06-06-285MOD. surgical instrument.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0939-2024·2024-03-06

    Food Recall: Quaker Chewy Bars Potentially Contaminated with Salmonella

    The Quaker Oats Company is recalling Quaker Chewy Bars and Dipps Variety Packs due to potential Salmonella contamination. The affected products were distributed nationally and internationally, and consumers should discard or return them.

    Product
    Quaker Chewy Bars and Dipps Variety Pack 14ct 13 oz and 58ct 58.6 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1194-2024·2024-03-06

    Integra Cranial Access Kit Recalled for Sterile Packaging Defect

    Integra LifeSciences is recalling 27 units of its Cranial Access Kit due to defective sterile packaging that may compromise product sterility. The kits were distributed worldwide.

    Product
    Ref No: HITHSP04 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0359-2024·2024-03-06

    7 Eleven Hand Sanitizer Gel recalled for manufacturing facility deficiencies

    Seatex LLC is recalling 1,282 cases of 7 Eleven Hand Sanitizer Gel due to manufacturing facility deficiencies found during FDA inspection. The product was distributed nationwide.

    Product
    7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1196-2024·2024-03-06

    Integra cranial access kit recalled for sterile packaging failure

    Integra LifeSciences is recalling 1,324 cranial access kits due to sterile packaging defects that may compromise product sterility.

    Product
    Ref No: INS5HND / Integra Cranial access kit (without Prep solutions) Bit and Guard. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0353-2024·2024-03-06

    CVS Health Lubricant Eye Ointment recalled due to lack of sterility assurance

    CVS Health Lubricant Eye Ointment is being recalled nationwide due to lack of sterility assurance during manufacturing. The recall affects 159,334 units distributed in 3.5-gram tubes with lot numbers A2F03, A2I02, A2L02, A3C04, and A3H04.

    Product
    CVS Health Lubricant Eye Ointment (Mineral oil 31.9% Emollient, White petrolatum 57.7% Emollient), Packaged in in 3.5 gram tubes, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, NDC 76168-707-35, UPC 050428634141
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1209-2024·2024-03-06

    Colonoscope Recall: Missing Protective Adhesive May Cause Device Failure

    Olympus Corporation is recalling 18 colonoscopes with missing adhesive that protects against physical stress. The missing protective adhesive could allow device failure under vibration, temperature fluctuation, or shock.

    Product
    Colonoscope, Model Number PCF-H180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0944-2024·2024-03-06

    Quaker Chewy Bars Chocolate Chip recalled for potential Salmonella

    The Quaker Oats Co. is recalling Quaker Chewy Bars Chocolate Chip Spring Minis nationwide due to potential Salmonella contamination. Affected products have a Best Before date of August 2, 2024, or earlier.

    Product
    Quaker Chewy Bars Chocolate Chip Spring Minis 28ct 13.8 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0966-2024·2024-03-06

    Quaker On The Go Snack Mix recalled due to potential Salmonella contamination

    The Quaker Oats Co. is recalling Quaker On The Go Snack Mix products due to potential Salmonella contamination. A total of 22,512,942 cases are affected, distributed in all states, Puerto Rico, Guam, and Saipan, as well as internationally, with a Best Before date of Aug-02-24 or earlier.

    Product
    Quaker On The Go Snack Mix; 20ct Box 344 oz
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·24V314000·2024-03-05

    Airstream Atlas Motorhome Generator Recalled for Missing Heat Shield

    Certain 2023-2024 Airstream Atlas motorhomes may lack a heat shield on the generator, exposing subflooring to excessive heat. This defect increases the risk of fire and injury.

    Product
    AIRSTREAM — 2023 AIRSTREAM ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V384000·2024-03-05

    Ford F-Series and E-Series Vehicles Missing Tire Information on Safety Labels

    Ford is recalling certain 2022 F-Series and 2023 E-Series vehicles whose Safety Certification Labels are missing tire size, rim type, and pressure values. The missing information could lead to incorrect tire selection or pressure, increasing crash risk.

    Product
    FORD — 2022 FORD F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V385000·2024-03-05

    Roadtrek Recreational Vehicles Cooktop Recalled Due to Gas Leak Fire Risk

    Roadtrek is recalling 2021-2022 recreational vehicles with 2-burner cooktops that may develop gas leaks from damaged valves, increasing fire risk. Owners should contact Roadtrek customer service at 1-888-762-3873 for free cooktop replacement.

    Product
    ROADTREK — 2021 ROADTREK SS AGILE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V381000·2024-03-05

    Forest River Berkshire Motorhomes Recalled for Circuit Breaker Fire Hazard

    Forest River is recalling certain 2021-2022 Berkshire motorhomes with an incorrect circuit breaker installed in the electrical system. The defect can cause excessive heat and create a fire risk.

    Product
    FOREST RIVER — 2022 FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V249000·2024-03-04

    2023-2024 Aston Martin DBX Oil Cooler Hoses May Burst

    Aston Martin is recalling certain 2023-2024 DBX707 vehicles because oil cooler hoses may burst, causing sudden oil loss that could lead to engine failure and fire.

    Product
    ASTON MARTIN — 2023 ASTON MARTIN DBX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V282000·2024-03-04

    Commercial buses with inoperative collision system lack required warning label

    Navistar is recalling certain 2022-2023 commercial buses equipped without forward radar units. The required warning label indicating the collision mitigation system is inoperative may be missing, increasing crash risk.

    Product
    IC BUS — 2022 IC BUS RE
    Category
    Vehicle
    Distribution
    Distributed nationwide