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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13726–13750 of 27735

  • HighFDA (Devices)·Z-1214-2024·2024-03-06

    Colonoscope Model PCF-Q180AL Recalled Due to Missing Protective Adhesive

    Olympus Corporation of the Americas is recalling Colonoscope Model PCF-Q180AL units that were assembled without protective adhesive. This missing adhesive protects the device from vibration, temperature fluctuations, and physical shock during use.

    Product
    Colonoscope, Model Number PCF-Q180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0949-2024·2024-03-06

    Quaker Chewy Bars Less Sugar Cookies & Cream Recalled for Potential Salmonella

    The Quaker Oats Co. has recalled Quaker Chewy Bars Less Sugar Cookies & Cream for potential Salmonella contamination. The product with Best Before dates of August 2, 2024, or earlier was distributed nationwide and internationally.

    Product
    Quaker Chewy Bars Less Sugar Cookies & Cream. 1ct 1.38 oz; 8ct 6.7 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0952-2024·2024-03-06

    Snack Bar Recall: Quaker Chewy Bars Oatmeal Raisin Due to Potential Salmonella

    The Quaker Oats Company is recalling Quaker Chewy Bars Oatmeal Raisin due to potential Salmonella contamination. The recall affects approximately 22.5 million cases distributed nationally and internationally.

    Product
    Quaker Chewy Bars Oatmeal Raisin 8ct 6.7 oz; 58ct 48.7 oz; 1ct 0.84 oz; 440ct 369.6 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1191-2024·2024-03-06

    Dialysis Accessory Device Recalled for Blood Leakage Risk

    The NxStage Cartridge Express dialysis device is recalled because blood can leak or spray from the arterial line. This could cause uncontrolled blood loss in patients or expose healthcare workers to infectious blood.

    Product
    NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and replacement of a flow-compromised filter during treatment of acute and chronic renal failure or fluid overload.
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Food)·F-0948-2024·2024-03-06

    Quaker Chewy Bars Less Sugar Chocolate Chip recalled for potential Salmonella

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

    Product
    Quaker Chewy Bars Less Sugar Chocolate Chip 8ct 6.7 oz; 18ct 15.1 oz; 58ct 48.7 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0943-2024·2024-03-06

    Quaker Chewy Bars recalled for potential Salmonella

    The Quaker Oats Company is recalling Quaker Chewy Bars Chocolate Chip Halloween Minis with Best Before dates of Aug-02-24 or earlier due to potential Salmonella. No illnesses have been reported.

    Product
    Quaker Chewy Bars Chocolate Chip Halloween Minis 28ct 13.8 oz; 40ct 19.6 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·22V458000·2024-03-06

    2020-2022 Hyundai Venue seat belt pretensioners may explode in crash

    Hyundai is recalling 2020-2022 Venue vehicles because the front seat belt pretensioners may explode when deployed in a crash, potentially projecting metal fragments at occupants.

    Product
    HYUNDAI — 2021 HYUNDAI VENUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1193-2024·2024-03-06

    Cranial Access Kit recalled due to sterile packaging integrity defect

    Integra LifeSciences is recalling a Cranial Access Kit due to packaging defects that may compromise sterility. The product was distributed worldwide.

    Product
    Ref No: 31156 / COMBO KIT CONTAINS INS-8301, INS-4500,INS-HITH. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V391000·2024-03-06

    2023 Nissan Ariya: Loss of Drive Power Due to Motor Assembly Defect

    Nissan is recalling certain 2023 Ariya vehicles with defective electric front traction motors. Damaged O-rings can cause internal oil leaks and unexpected loss of drive power, increasing crash risk.

    Product
    NISSAN — 2023 NISSAN ARIYA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1183-2024·2024-03-06

    Infusion Pumps Model Z-800WF Recalled Due to Alarm Volume Malfunction

    Zyno Medical recalls Z800 infusion pumps (Model Z-800WF) with software version 5.2.05 due to a potential alarm volume malfunction. The alarm may revert to low volume, delaying therapy and risking organ failure in extreme cases.

    Product
    Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide intravenous infusion of parenteral fluids, blood and blood products to a patient under the direction or supervision of physician or other certified health care professional Model: Z-800WF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0959-2024·2024-03-06

    Quaker Chewy Mini Dipps Summer Night S'mores bars recalled due to Salmonella risk

    The Quaker Oats Co. is voluntarily recalling Quaker Chewy Mini Dipps Summer Night S'mores bars due to potential Salmonella contamination. The recall affects products with Best Before dates of Aug-02-24 and earlier distributed nationally.

    Product
    Quaker Chewy Mini Dipps Summer Night S'mores 12ct 8.9 oz Bars are individually wrapped in plastic and then packaged in paperboard boxes.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0975-2024·2024-03-06

    Quaker Chewy Granola Bars Recalled for Potential Salmonella Contamination

    Quaker Oats is recalling Quaker Chewy Granola Bars (Fruity Fun) Amazing Apple due to potential Salmonella contamination. Affected products with Best Before dates of Aug-02-24 or earlier were distributed nationally and internationally.

    Product
    Quaker Chewy Granola Bars (Fruity Fun) Amazing Apple 0.84 oz 6 Count
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1210-2024·2024-03-06

    Olympus Colonoscope Recall: Missing Protective Adhesive in 47 Units

    Olympus is recalling 47 colonoscope units (Model PCF-H190DL) because they were assembled without protective adhesive. The missing adhesive may cause equipment failure under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number PCF-H190DL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0993-2024·2024-03-06

    Cap n Crunch Cinnamon Crunch Cereal Recalled for Potential Salmonella

    Cap n Crunch Cinnamon Crunch Cereal is being recalled due to potential Salmonella contamination. The recall affects products distributed nationally across all U.S. states and territories.

    Product
    Cap n Crunch Cinnamon Crunch Cereal 11.2 oz; 19.3 oz;
    Category
    Food
    Distribution
    0 states
  • 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 (Devices)·Z-1216-2024·2024-03-06

    USTAR II Knee System implants recalled for potential stem misalignment

    The FDA is recalling USTAR II Knee System implants due to potential incorrect orientation of the curved stem. The defect may affect proper implant positioning in knee replacement surgery.

    Product
    USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: REF: PE25153109 - 9x125mm, PE25153209 - 9x150mm, PE25153113 - 13x125mm, PE25153111- 11x125mm, PE25153115 - 15x125mm, PE25153211 - 11x150mm, PE25153213 - 13x150mm, PE25153217 - 17x1
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0936-2024·2024-03-06

    Quaker Big Chewy Bars Chocolate Chip recalled for potential Salmonella

    The Quaker Oats Company is voluntarily recalling Quaker Big Chewy Bars Chocolate Chip due to potential Salmonella contamination. The product, distributed nationwide and internationally, affected millions of cases.

    Product
    Quaker Big Chewy Bars Chocolate Chip 5ct 7.4 oz, 1ct 1.48 oz, 10ct 14.8 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0971-2024·2024-03-06

    Frito-Lay Snack Mix Variety Packs Recalled for Potential Salmonella

    The Quaker Oats Co. is recalling Frito-Lay Popped & Baked Chips variety packs for potential Salmonella contamination. Affected products have best-before dates of August 2, 2024 or earlier and were distributed nationally and internationally.

    Product
    Frito-Lay Popped & Baked Chips with Cookies, Nuts and Quaker Chewy Bars Variety Pack 40ct 35.58 oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1199-2024·2024-03-06

    Integra Cranial Access Kit recall over sterile packaging defect

    Integra LifeSciences is recalling the Cranial Access Kit due to a defect in the sterile packaging that may compromise product sterility. Affects 30 units distributed worldwide.

    Product
    Ref No: INS7270 / Integra¿ Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1201-2024·2024-03-06

    Integra Cranial Access Kit Recalled for Compromised Sterile Packaging

    Integra LifeSciences is recalling 8,906 units of the Cranial Access Kit because the sterile packaging failed integrity testing, potentially compromising sterility. Units were distributed worldwide.

    Product
    Ref No: INSHITH / Integra¿ Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-0932-2024·2024-03-06

    Chin Jung White Kimchi Recalled Due to Undeclared Fish Allergen

    Chin Jung White Kimchi jars recalled due to undeclared fish allergen. Products distributed to supermarkets in California, Colorado, and Nevada may pose risk to consumers with fish allergies.

    Product
    Chin Jung White Kimchi - 7 lb. 8 oz.(3.4 kg) plastic jars
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0994-2024·2024-03-06

    Cap n Crunch Sea Berry Crunch Cereal Recalled Due to Potential Salmonella

    The Quaker Oats Co. is voluntarily recalling Cap n Crunch Sea Berry Crunch Cereal 15.5 oz boxes due to potential Salmonella contamination. The recalled products have a Best Before date of Aug-02-24 or earlier.

    Product
    Cap n Crunch Sea Berry Crunch Cereal 15.5 oz
    Category
    Food
    Distribution
    0 states