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

17451–17475 of 114193

  • SevereFDA (Devices)·Z-1057-2024·2024-03-06

    AirLife Adult Manual Resuscitator units recalled for component failure

    Vyaire Medical is recalling 106,656 units of AirLife Adult Manual Resuscitator bags due to faulty components that may break during use, causing ventilation failure and potentially leading to hypoxia or death.

    Product
    AirLife Adult Manual Resuscitator, Oxygen Reservoir Bag, without Mask, REF 2K8000,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1162-2024·2024-03-06

    Medtronic Duet External Drainage System Recalled for Catheter Disconnection Risk

    Medtronic is recalling 30,711 units of its Duet External Drainage System because of the potential for catheter disconnection from patient line stopcock connectors.

    Product
    Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce intracranial pressure and CSF volume.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0981-2024·2024-03-06

    Cap'n Crunch Treats cereal bars recalled nationwide for potential Salmonella

    Quaker Oats is recalling Cap'n Crunch Treats Crunch Berries cereal bars due to potential Salmonella contamination. The affected products have a Best Before date of Aug-02-24 or earlier and were distributed nationwide.

    Product
    Cap'n Crunch Treats Crunch Berries Cereal Bar 0.84 oz 8 Count; 2.11 oz 1 Count; 1.79 oz 12 Count; 0.84 oz 16 Count
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0961-2024·2024-03-06

    Quaker Puffed Granola Blueberry Vanilla Cereal Recall for Salmonella

    The Quaker Oats Co. recalled Quaker Puffed Granola Blueberry Vanilla Cereal (17 oz) due to potential Salmonella contamination. Products with Best Before dates of Aug-02-24 and earlier may be affected.

    Product
    Quaker Puffed Granola Blueberry Vanilla Cereal; 17 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0350-2024·2024-03-06

    Mesalamine extended-release capsules recalled due to dissolution failure

    Sun Pharmaceutical is recalling Mesalamine extended-release capsules due to failed dissolution specifications. The affected capsules may not dissolve and release medication properly.

    Product
    MESALAMINE — MESALAMINE (MESALAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0991-2024·2024-03-06

    Breakfast Cereal Recall: Quaker Oatmeal Squares for Potential Salmonella

    The Quaker Oats Co. is recalling Quaker Oatmeal Squares Breakfast Cereal due to potential Salmonella contamination. The product was distributed nationally and internationally.

    Product
    Quaker Oatmeal Squares Breakfast Cereal, Variety Pack 43.5 oz 3 Pack
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1207-2024·2024-03-06

    Colonoscope Model CF-HQ190L Recalled Due to Missing Protective Adhesive

    Olympus Corporation is recalling 97 Colonoscope Model CF-HQ190L units distributed nationwide. The devices were assembled without protective adhesive, risking malfunction under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number CF-HQ190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1205-2024·2024-03-06

    Colonoscope Model CF-H180AL Recalled Due to Missing Protective Adhesive

    Olympus is recalling 36 colonoscopes with specific serial numbers that lack a protective adhesive, risking device failure if exposed to vibration, temperature changes, or shock loads.

    Product
    Colonoscope, Model Number CF-H180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1219-2024·2024-03-06

    Hip Implant Component Mislabeled With Wrong Insert Type on Packaging

    LINK BiMobile hip implant liners are being recalled because packaging incorrectly identifies the insert type as F instead of G. This labeling error could delay surgery or result in the wrong component being used.

    Product
    LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0957-2024·2024-03-06

    Quaker Chewy Dipps snack bars recalled for potential Salmonella contamination

    The Quaker Oats Company is voluntarily recalling Quaker Chewy Dipps Variety Pack snack bars due to potential Salmonella contamination. The recall affects products distributed nationally across all U.S. states, territories, and some international markets.

    Product
    Quaker Chewy Dipps Variety Pack 14ct 15 oz; 48ct 51.6 oz Bars are individually wrapped in plastic and then packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1198-2024·2024-03-06

    Integra Cranial Access Kit recalls due to packaging sterility defect

    Integra LifeSciences is recalling 161 units of the Cranial Access Kit (Lot 7124720) due to packaging defects that may compromise sterility. The recall affects units distributed worldwide.

    Product
    Ref No: INS7260 / 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-0972-2024·2024-03-06

    Frito-Lay Snack Time Favorites Variety Pack Recalled for Potential Salmonella

    Frito-Lay has recalled Snack Time Favorites variety packs due to potential Salmonella contamination. Affected products have a Best Before date of August 2, 2024 or earlier and were distributed nationally and internationally.

    Product
    Frito-Lay Snack Time Favorites with Baked, Smartfood, SunChips and Quaker Chewy Granola Bars Variety Pack 40ct 33.94 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0942-2024·2024-03-06

    Quaker Chewy Bars Chocolate Chip Holiday Minis recalled for potential Salmonella

    The Quaker Oats Co. is recalling Quaker Chewy Bars Chocolate Chip Holiday Minis due to potential Salmonella contamination. The recall affects products with Best Before dates of Aug-02-24 and earlier, distributed nationwide and internationally.

    Product
    Quaker Chewy Bars Chocolate Chip Holiday Minis 28ct 13.8 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1211-2024·2024-03-06

    Colonoscope Model PCF-H190L Recalled for Missing Protective Adhesive

    Olympus Corporation recalled 31 colonoscopes lacking a protective adhesive that shields against vibration, temperature fluctuations, and shock. The missing adhesive may affect device structural integrity under physical stress.

    Product
    Colonoscope, Model Number PCF-H190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0989-2024·2024-03-06

    Food recall: Quaker Oatmeal Squares due to potential Salmonella

    Quaker Oats Co. is recalling Quaker Oatmeal Squares Brown Sugar in multiple sizes due to potential Salmonella contamination. Affected products have Best Before dates of Aug-02-24 or earlier and were distributed nationally and internationally.

    Product
    Quaker Oatmeal Squares Brown Sugar 14.5 oz; 21 oz; 43.5 oz 3 Pack; 29 oz 2 Count
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0970-2024·2024-03-06

    Food recall: Quaker Oats snack variety pack due to potential salmonella

    The Quaker Oats Co. recalls Lunch Box Mix Frito-Lay Chips, Cookies and Quaker Chewy Bars Variety Pack (40ct, 40.62 oz) due to potential Salmonella contamination. The product was distributed nationally and internationally.

    Product
    Lunch Box Mix, Frito-Lay Chips, Cookies and Quaker Chewy Bars Variety Pack 40ct 40.62 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0992-2024·2024-03-06

    Cereal Recall: Cap n Crunch OOPS! All Berries Due to Salmonella Risk

    The Quaker Oats Co. is recalling Cap n Crunch OOPS! All Berries Cereal (10.3 oz) due to potential Salmonella contamination. Products with a Best Before date of Aug-02-24 or earlier are affected nationally.

    Product
    Cap n Crunch OOPS! All Berries Cereal 10.3 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0363-2024·2024-03-06

    Lidocaine and Phenylephrine Injectable Vials Recalled for Glass Delamination

    Denver Solutions is recalling Lidocaine-Phenylephrine injectable vials nationwide due to glass delamination in the vials. The defect could potentially introduce glass fragments into the medication.

    Product
    Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0983-2024·2024-03-06

    Cap'n Crunch cereal bars recalled for potential Salmonella contamination

    The Quaker Oats Company recalled Cap'n Crunch Treats Peanut Butter Crunch Cereal Bars due to potential Salmonella contamination. Affected products have a Best Before date of August 2, 2024 or earlier.

    Product
    Cap'n Crunch Treats Peanut Butter Crunch Cereal Bar 0.84 oz 8 Count; 2.11 oz 1 Count; 2.11 oz 12 Count;
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0995-2024·2024-03-06

    Cereal Recall: Gamesa Marias Due to Potential Salmonella

    The Quaker Oats Co. is recalling Gamesa Marias Cereal due to potential Salmonella contamination. The recall affects products distributed nationwide and internationally with a Best Before date of Aug-02-24 or earlier.

    Product
    Gamesa Marias Cereal 11.4 oz and 11.4 oz 2 count
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1001-2024·2024-03-06

    Reser's Amish Macaroni Salad recalled for undeclared wheat allergen

    Reser's Amish Macaroni Salad is recalled because some containers have a mislabeled side label that does not declare wheat, which is an ingredient in the product. This poses a risk to people with wheat allergies.

    Product
    The recalled Reser's Amish Macaroni Salad was packaged in a plastic clear container where the top lid is labeled as Reser's Amish Macaroni Salad, Net Wt. 1lb., and the container side label indicates Reser s Southern Style with Egg Potato Salad, Net Wt. 1lb. UPC 0 71117 19044 1.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0980-2024·2024-03-06

    Quaker Chewy Granola Bars recalled for potential Salmonella contamination

    The Quaker Oats Co. is recalling Quaker Chewy Granola Bars Yogurt Variety Packs due to potential Salmonella contamination. Affected products have Best Before dates of Aug-02-24 or earlier and were distributed nationally and internationally.

    Product
    Quaker Chewy Granola Bars Yogurt Variety Packs 1.23 oz 10 Count; 1.23 OZ 21 Count; 41.8 oz 34 Count; 1.23 oz 14 Count
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0958-2024·2024-03-06

    Quaker Chewy Mini Dipps Birthday Blast bars recalled for potential Salmonella

    Quaker Oats is voluntarily recalling Quaker Chewy Mini Dipps Birthday Blast bars for potential Salmonella. The recall covers products with Best Before dates of Aug 2, 2024 and earlier distributed nationally.

    Product
    Quaker Chewy Mini Dipps Birthday Blast 12ct 8.9 oz Bars are individually wrapped in plastic and then packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1202-2024·2024-03-06

    Integra Cranial Access Kit Recalled for Defective Sterile Packaging

    Integra LifeSciences is recalling 915 units of its Cranial Access Kit worldwide due to defective sterile packaging that may compromise product sterility. The header bags failed required packaging integrity testing.

    Product
    Ref No: INSHITHND / 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-0354-2024·2024-03-06

    FDA recalls Lubricant PM Ointment due to sterility assurance failure

    Lubricant PM Ointment is being recalled by AACE Pharmaceuticals due to the manufacturer's failure to assure the product was manufactured under sterile conditions.

    Product
    Lubricant PM Ointment (Mineral Oil 42.5% and White Petrolatum 57.3%), Packaged in 3.5 gram tubes, Distributed by: AACE Pharmaceuticals, Inc., Fairfield, NJ 07004, NDC 71406-124-35, UPC 371406124356
    Category
    Drug
    Distribution
    Distributed nationwide