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

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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

27676–27681 of 27681

  • HighFDA (Devices)·Z-1788-2012·2012-06-20

    GE Healthcare Revolution XR/d Recalled for Finger Pinch Hazard

    General Electric is recalling 3,796 Revolution XR/d digital radiographic imaging systems worldwide due to a reported incident where an operator's finger was pinched.

    Product
    GE Healthcare Revolution XR/d; GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model numbers: 2259988-2 & 2351505. The Revolution XR/d Digital Radiographic Imaging System is indicated for use in generating radiographic images of human anatomy. It is intended to…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1789-2012·2012-06-20

    GE Healthcare Definium 8000 Digital Radiographic Systems Recalled for Pinch Hazard

    General Electric is recalling 3,796 Definium 8000 Digital Radiographic Systems because an operator's finger was pinched between the fixed roller and the gliding tabletop.

    Product
    GE Healthcare Definium 8000 Digital Radiographic Systems : GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model Number: 5131070. The Revolution XR/d with Tomosynthesis is intended for use in generating Tomographic images of human anatomy. It is not intended for…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1792-2012·2012-06-20

    MicroAire Lipofilter 3000 Canisters Recalled for Sterilization Defects

    MicroAire Surgical Instruments is recalling 15 Lipofilter 3000 fat collection canisters because they were not manufactured under Good Manufacturing Procedures, potentially preventing proper sterilization.

    Product
    Lipofilter 3000, model ASP-CAN-2, labeled in part ***MicroAire, 1641 Edlich Drive, Charlottesville, VA 22911, USA*** Product Usage: A fat collection canister intended for use during liposuction procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1538-2012·2012-06-20

    Philips Healthcare Recalls Mobile X-ray Systems Due to Unintended Radiation

    Philips Healthcare is recalling 11 mobile X-ray systems because they may generate unintended radiation pulses when switched off or parked.

    Product
    Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1793-2012·2012-06-20

    Aesculap Recalls Columbus Tibia Plateau Components Due to Specification Defects

    Aesculap Implant Systems is recalling eight Columbus Tibia Plateau components because they were found out of specification during internal quality inspection.

    Product
    Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Columbus Revision Knee System is indicated for use in reconstruction of the diseased knee joint caused by osteoarthritis, rheumatoid arthritis, post-traumatic arthritis, the need to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1790-2012·2012-06-20

    GE Proteus XR/a Radiographic System Recalled Due to Pinch Hazard

    General Electric is recalling 3,796 Proteus XR/a Radiographic Systems worldwide because an operator's finger was pinched between the fixed roller and the gliding tabletop.

    Product
    GE Proteus XR/a Radiographic System. GE Medical Systems-Americas Milwaukee, WI. Model Number: 2259988. Product is indicated for use in generating radiographic images of human anatomy in all general-purpose diagnostic procedures. This device is not intended for mammographic…
    Category
    Medical Device
    Distribution
    0 states