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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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

17301–17325 of 27769

  • HighFDA (Drugs)·D-0915-2023·2023-07-19

    Hand Sanitizer Recalled for Impurities Exceeding Allowable Limits

    Big Machine Distillery Hand Sanitizer is being recalled due to manufacturing impurities exceeding allowable limits. No illnesses or injuries have been reported.

    Product
    Big Machine Distillery Hand Sanitizer Non-Sterile Solution Alcohol Antiseptic 80% Topical Solution, Produced and Distributed by Big Machine Distillery 1800 Abernathy Road Lynnville, TN 38472 a) 50 mL UPC 8 59105 00452 5; b) 100 mL UPC 8 59105 00453 2; c) 375 mL; d) 1/2 gallon; e)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-2107-2023·2023-07-19

    Orthopedic Screw Recall Due to Undersized Head in Surgical Device

    Osteomed is recalling orthopedic screws with undersized heads that may pass through bone plates. Affected lot numbers were distributed nationwide in the US and Singapore.

    Product
    REF: 218-1604, 1.6mm x 4mm Profile Zero Auto-Drive Screw, Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2023·2023-07-19

    Medtronic Catalyft LS Spinal Implant Recall Due to Out-of-Specification Geometry

    Medtronic recalls 10 units of Catalyft LS spinal implants due to potential out-of-specification device geometries. The affected implants may not properly support or accommodate patient anatomy during lumbar fusion surgery.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027722, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2109-2023·2023-07-19

    Surgical chest support device recalled for potential cracking at attachment

    Baxter Healthcare recalls 1,010 Allen Advance Chest Support devices due to potential cracking where the support attaches to operating room table rails. No injuries reported.

    Product
    Allen Advance Chest Support with Pad
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2119-2023·2023-07-19

    Medtronic Catalyft LS Spinal Implants Recalled for Out-of-Specification Dimensions

    Medtronic recalls 25 units of Catalyft LS spinal implants (lot numbers NM21J039, NM21M026) due to out-of-specification device dimensions that may affect surgical fit and function.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981025522, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0900-2023·2023-07-19

    BASIC CARE Allergy Tablets Recalled Due to Failed Quality Specifications

    BASIC CARE ALLERGY (fexofenadine hydrochloride) 180 mg tablets are being recalled nationwide due to failed impurities and product degradation specifications. Approximately 11,904 cartons were affected.

    Product
    BASIC CARE ALLERGY — BASIC CARE ALLERGY (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·23244·2023-07-13

    Frigidaire Gas Laundry Centers Recalled Due to Fire Hazard

    Electrolux Group is recalling about 13,600 Frigidaire Gas Laundry Centers because the felt seal on the dryer drum can fold inward, causing lint to accumulate and creating a fire hazard. The company has received 23 reports of fire and one report of smoke inhalation injury.

    Product
    Frigidaire Gas Laundry Centers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23243·2023-07-13

    Gas-Fired Residential Boilers Recalled for Carbon Monoxide Exposure Risk

    ECR International is recalling about 1,745 gas-fired hot water residential boilers that may be missing a flue inspection cover plate, which can expose residents to combustion flue gases and carbon monoxide poisoning.

    Product
    Gas-fired hot water residential boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23773·2023-07-13

    Yamaha Personal Transportation Vehicles Recalled for Unexpected Acceleration Hazard

    Yamaha is recalling approximately 370 personal transportation vehicles sold nationwide from August 2022 through March 2023 because they can accelerate unexpectedly, creating crash and injury hazards.

    Product
    Yamaha Personal Transportation Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1102-2023·2023-07-12

    Breader product recalled due to potential Salmonella contamination

    Newly Weds Foods is recalling over 6.4 million pounds of breader product that may contain Salmonella. The product was distributed across 28 U.S. states and Canada.

    Product
    B93386 BREADER X1 50.00 BAG
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1154-2023·2023-07-12

    Burgundy Pepper Inject Recalled for Potential Salmonella Contamination

    Newly Weds Foods is recalling Burgundy Pepper Inject P2 due to potential Salmonella contamination. The product was distributed across 28 states and Canada.

    Product
    G70508 BURGUNDY PEPPER INJECT P2 25.00 BOX
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1168-2023·2023-07-12

    Newly Weds Foods Pastrami Rub Recalled for Potential Salmonella

    Newly Weds Foods is recalling EMMPAK Pastrami Rub across 28 US states and Canada due to potential Salmonella contamination. Lot codes SE278179 and SE282397 are affected.

    Product
    G92362 EMMPAK PASTRAMI RUB 30.00 BOX
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1125-2023·2023-07-12

    Roast Pork Seasoning Rub Recalled Due to Salmonella Contamination

    Newly Weds Foods, Inc. is recalling roast pork seasoning rub products that may contain Salmonella. The recall affects products distributed across multiple U.S. states and Canada.

    Product
    G22041 ROAST PORK SEASONING RUB 25.00 CASE
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1194-2023·2023-07-12

    BBQ Seasoning Recalled Due to Possible Salmonella Contamination

    Newly Weds Foods is recalling Chix BBQ Seasoning due to possible Salmonella contamination. The product was distributed to 28 US states and Canada.

    Product
    S02192 CHIX BBQ SEASONING X1 52.72 BAG
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1177-2023·2023-07-12

    Lotta Zing Sauce Mix recalled for potential Salmonella contamination

    Newly Weds Foods is recalling Lotta Zing Sauce Mix due to potential Salmonella contamination. Consumers with affected products should not use them.

    Product
    G96378 LOTTA ZING SAUCE MIX X2 15.00 CASE
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1153-2023·2023-07-12

    Newly Weds Foods spice blend recalled for potential salmonella contamination

    Newly Weds Foods is recalling its Turkey Burger Spice Blend (G68631) across multiple U.S. states and Canada due to potential salmonella contamination. Approximately 6.4 million pounds are affected.

    Product
    G68631 TURKEY BURGER SPICE BLEND X3 50.00 BAG
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1110-2023·2023-07-12

    Breader Product Recall Due to Salmonella Contamination Risk

    Newly Weds Foods is recalling breader products that may contain Salmonella. The recall affects products distributed across 27 US states and Canada.

    Product
    B97705 BREADER X3 50.00 BAG
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1034-2023·2023-07-12

    Newly Weds Foods Batter Mix Recalled for Potential Salmonella Contamination

    Newly Weds Foods, Inc. is recalling approximately 6.5 million pounds of batter mix due to potential Salmonella contamination. The product was distributed across 28 U.S. states and Canada.

    Product
    A28460 BATTER MIX X1 50.00 BAG
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1038-2023·2023-07-12

    Seasoned Flour Recalled Due to Potential Salmonella Contamination

    Newly Weds Foods is recalling A52541 seasoned flour (product code MT110322C) due to potential Salmonella contamination. The product has been distributed across the United States and Canada.

    Product
    A52541 SEASONED FLOUR X1 50.00 BAG
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1026-2023·2023-07-12

    Batter Mix Products Recalled for Potential Salmonella Contamination

    Newly Weds Foods is recalling A20180 Batter Mix in 50-pound bags due to potential Salmonella contamination. The recall affects products distributed across 28 US states and Canada.

    Product
    A20180 BATTER MIX X4 50.00 BAG
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1047-2023·2023-07-12

    W Crispy Chicken Batter Mix recalled due to Salmonella contamination risk

    Newly Weds Foods, Inc. is recalling W Crispy Chicken Batter Mix due to potential Salmonella contamination. The product was distributed across multiple U.S. states and Canada.

    Product
    A86554 W CRISPY CHICKEN BATTER MIX X2 50.00 BAG
    Category
    Food
    Distribution
    0 states