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

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

26126–26150 of 90150

  • HighFDA (Devices)·Z-0830-2022·2022-04-06

    Siemens Magnesium Flex reagent cartridge recalled for imprecision and assay errors

    Siemens recalls magnesium reagent cartridges due to imprecision and abnormal assay flags that may cause erroneous diagnostic results and require repeat patient testing.

    Product
    Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the Dimension Vista System. The Dimension Vista Magnesium Flex Reagent (MG) method is an In vitro diagnostic test for the quantitative measurement of magnesium in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0847-2022·2022-04-06

    BALLARD Multi-Access Port Catheter Recalled for Incorrect Expiration Date

    Avanos Medical is recalling 2,520 BALLARD Multi-Access Port Catheters due to incorrect expiration dates on the packaging. No illnesses or injuries have been reported. Patients should verify the lot number and contact their healthcare provider.

    Product
    BALLARD* Multi-Access Port (MAP) Catheter, Double Swivel Y- Adult, 16 French; Sterile; Single Use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0736-2022·2022-04-06

    Glycopyrrolate Tablets Recalled Due to Glass Pieces in Sealed Bottles

    Aurolife Pharma is recalling Glycopyrrolate Tablets after glass fragments were discovered in a sealed bottle from packaging equipment. Approximately 4,080 bottles were distributed nationwide and in Puerto Rico.

    Product
    GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0835-2022·2022-04-06

    Tissue oximeter module may provide inaccurately low oxygen readings

    Edwards Lifesciences is recalling 8,389 FORE-SIGHT ELITE Tissue Oximeter modules that may display inaccurately low oxygen saturation values when used in certain body locations, potentially leading to inappropriate treatment decisions.

    Product
    FORE-SIGHT ELITE Tissue Oximeter module, REF: HEMFSM10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0960-2022·2022-04-06

    Good & Gather Dried Strawberries Recalled for Undeclared Sulfites

    Good & Gather Dried Sweetened Strawberries are being recalled due to undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.

    Product
    Good & Gather Dried Sweetened Strawberries. Net Wt 4 oz (113g). UPC 085239-182840 No Sulfites Added. No Artificial Flavors. No Synthetic Colors. Distributed by Target Corporation, Minneapolis, MN 55403
    Category
    Food
    Distribution
    20 states
  • HighFDA (Food)·F-0916-2022·2022-04-06

    Carbquik Complete Biscuit Mix Recalled for Undeclared Milk Allergen

    Tova Industries Inc is recalling Carbquik Complete Biscuit and Baking Mix due to undeclared milk allergen. The recall affects 224 cases distributed through an Amazon distribution center in New Mexico.

    Product
    Carbquik Complete Biscuit and Baking Mix, Net Wt. 3lb *Contained 1 free sample of Cinnamon Spice Mug Cake
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0917-2022·2022-04-06

    Tam's Homemade Biscuits recalled for missing allergen and ingredient labels

    Tam's Homemade Biscuits (Batch No. 015-022) are recalled due to missing allergen statement and ingredient list. Consumers with food allergies cannot identify potential allergens in the product.

    Product
    Tam's Homemade Biscuits 8 count packaged in 9 inch round aluminum cake pan 10 pans per case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0834-2022·2022-04-06

    FORE-SIGHT ELITE Tissue Oximeter: Inaccurate Oxygen Saturation Readings

    Edwards Lifesciences FORE-SIGHT ELITE Absolute Tissue Oximeter (Model 01-06-3000) is recalled because StO2 (tissue oxygen saturation) values may read inaccurately low when used with the large sensor on arms or legs, potentially leading to inappropriate treatment.

    Product
    FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0853-2022·2022-04-06

    Surgical Drill System Instrument Pack Recalled Over Device Breakage Risk

    Wright Medical is recalling 176 packs of the EasyFuse Dynamic Compression System Instrument Pack due to risk that the drill guide can jam and break during surgery.

    Product
    EasyFuse Dynamic Compression System Instrument Pack
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Drugs)·D-0732-2022·2022-04-06

    Testosterone Cypionate Injectable Recalled Due to Lack of Sterility Assurance

    Drug Depot, Inc. is recalling 620 vials of Testosterone Cypionate/DHEA injectables due to lack of sterility assurance in manufacturing. The product was distributed nationwide.

    Product
    TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable, Packaged in a multi dose 10ML vial, as a) 5 ML Formula ID 115678; b) 10 ML Formula ID 115498, APS Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0728-2022·2022-04-06

    FDA Recalls Gonadorelin Injectable Vials for Lack of Sterility Assurance

    Drug Depot, Inc. is recalling Gonadorelin 0.2 mg/mL injectable vials distributed nationwide due to lack of sterility assurance. Approximately 6,017 vials are affected.

    Product
    GONADORELIN (5ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID132227, APS Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0841-2022·2022-04-06

    Radiographic system software error may cause unintended tube stand movement

    Siemens is recalling 70 Ysio radiographic systems due to a software error that may cause unintended tube stand movement and create collision risk.

    Product
    Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0842-2022·2022-04-06

    Ceramic Hip Femoral Head Component May Not Match Package Label

    Howmedica Osteonics is recalling certain Biolox delta Ceramic V40 Femoral Head components because the actual size and offset may not match the package label. Patients with these implants should contact their surgeon.

    Product
    Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V219000·2022-04-05

    Land Rover Recalls 2016-2017 Range Rovers for Seat Belt Defect

    Jaguar Land Rover is recalling 2016-2017 Range Rover and Range Rover Sport vehicles because the driver's seat belt retractor may not lock during hard braking.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V216000·2022-04-01

    2021-2022 Autocar XPEDITOR vehicles recalled for ABS wiring defect

    Autocar is recalling 2021-2022 XPEDITOR vehicles because the ABS modulation valve may be wired incorrectly, potentially extending braking distance and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V215000·2022-04-01

    Mercedes-Maybach S 580 Recalled for Front Seat Trim Detachment Risk

    Mercedes-Benz is recalling 2021-2022 Maybach S 580 vehicles because front seat trim parts may detach during rear air bag deployment, potentially causing improper air bag function and injury.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH S 580, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E029000·2022-03-31

    GM Recalls Truck Hero Tonneau Covers for Detachment Risk

    General Motors is recalling specific Truck Hero tonneau covers for 2019-2022 Chevrolet and GMC trucks because they may detach while driving, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V210000·2022-03-31

    Chevrolet Traverse roof rail air bag harness connector defect

    General Motors is recalling certain 2020-2022 Chevrolet Traverse and 2021-2022 Buick Enclave vehicles because the harness connector to the roof rail air bags may have incompatible electrical terminals that could prevent air bag deployment in a crash.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V212000·2022-03-31

    Jayco Recalls 2022 White Hawk Travel Trailers Due to Fire Risk

    Jayco is recalling 2022 White Hawk travel trailers because loose power inlet wiring may cause an electrical arc or short, increasing the risk of a fire.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22737·2022-03-31

    SOUNDBOKS Gen. 3 Bluetooth Speakers Recalled for Battery Fire Hazard

    SOUNDBOKS Inc. is recalling about 6,700 Gen. 3 Bluetooth speakers because the removable lithium-ion battery can overheat and pose a fire hazard. Consumers should stop using the speakers immediately and contact the company for a free replacement battery.

    Product
    SOUNDBOKS (Gen. 3) Bluetooth Speakers with Lithium-Ion Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide