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.

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20126–20150 of 27682

  • HighFDA (Devices)·Z-1357-2017·2017-03-08

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES Recalled for Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Percutaneous Entry Kit, part number TVS4022(D Percutaneous Entry Kit , part number TVS4022(E Percutaneous Entry Kit, part number TVS4022(F
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1340-2017·2017-03-08

    Medtronic Gloves in AMS Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 39 Major Pack kits containing Medtronic gloves that may have splits or holes compromising sterility.

    Product
    Major Pack (1345), part number AMS6565
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1354-2017·2017-03-08

    Windstone Medical Recalls Ortho Minor Packs Due to Sterility Compromise

    Windstone Medical Packaging is recalling 664 Ortho Minor Packs because the included disposable gloves may contain splits or holes that compromise sterility.

    Product
    Ortho Minor Pack, part number AMS3710(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1342-2017·2017-03-08

    Windstone Medical Minor Procedure Packs Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 365 Minor Procedure Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Minor Procedure Pack, part number AMS4799
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1261-2017·2017-03-08

    Windstone Medical Arthroscopy Packs Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 1,081 arthroscopy kits because the disposable gloves inside may have splits or holes that compromise sterility.

    Product
    Arthroscopy Pack, part number AMS2938 Arthroscopy Pack, part number AMS3639 Arthroscopy Pack, part number AMS4765 Arthroscopy Pack, part number PSS1799 Arthroscopy Pack, part number PSS1845(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1305-2017·2017-03-08

    Windstone Medical Packaging Recalls General Packs with Defective Gloves

    Windstone Medical Packaging is recalling 1,501 General Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General Pack, part number AMS5341 General Pack, part number AMS5694
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1390-2017·2017-03-08

    Cook Inc. Recalls Flexor Radial Access Sets Due to Blood Loss Reports

    Cook Inc. is recalling 41,975 Flexor Radial Access Sets because a specific hemostatic valve design is associated with increased reports of blood loss.

    Product
    Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1298-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Eye Plastic Tray, part number PSS1931(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1339-2017·2017-03-08

    Windstone Medical Recalls Major Laparotomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 32 Major Laparotomy Packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Major Laparotomy Pack - NS, part number AMS4347
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1278-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Breast Recon Pack, part number AMS5698 Breast Recon Pack, part number AMS5698(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1361-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.

    Product
    Plastic Pack, part number PSS2462 Plastic Pack, part number PSS3319 Plastic Pack, part number PSS3319(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1385-2017·2017-03-08

    Merge Healthcare Recalls Unity PACS Software Due to Image Error

    Merge Healthcare is recalling Unity PACS software versions 11.0 and 11.0.1 because the software fails to add the correct tomo image.

    Product
    DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a…
    Category
    Medical Device
    Distribution
    Distributed nationwide