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

20101–20125 of 27647

  • 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
  • HighFDA (Devices)·Z-1386-2017·2017-03-08

    Maquet CARDIOSAVE IABP Li-Ion Battery Recall Due to Venting Risk

    Maquet is recalling Li-Ion batteries for CARDIOSAVE IABP devices after reports of venting when dropped.

    Product
    CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part number is 0146-00-0097 Product Usage: The CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2017·2017-03-08

    FDA Recalls Custom Breast Augmentation Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 229 Custom Breast Augmentation Packs because the included gloves may have splits or holes that compromise sterility.

    Product
    Custom Breast Augmentation Pack, part number PSS2455(D
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1253-2017·2017-03-08

    Phadia Recalls EliA Sample Diluent Due to Liquid Level Detection Issues

    Phadia US Inc is recalling EliA Sample Diluent because liquid level detection problems in Phadia 250 instruments caused erroneous test results.

    Product
    EliA Sample Diluent, Article number, 83-1023-01
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1383-2017·2017-03-08

    Synthes Recalls Mislabelled PRODISC Orthopedic Spinal Surgery Struts

    Synthes (USA) Products LLC is recalling two PRODISC Orthopedic Manual Surgical Instrument struts used in spinal surgery because they are incorrectly etched and labeled with the wrong size.

    Product
    PRODISC Orthopedic Manual Surgical Instrument, strut used in spinal surgery. Part numbers 03.820.350 and 03.820.352. Used to hold the disc segment open and facilitate discectomy
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1381-2017·2017-03-08

    Medtronic Gloves in Custom Kits Recalled for Sterility Compromise

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

    Product
    Vein Tray, part number AMS6312
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1258-2017·2017-03-08

    Windstone Medical Abdominoplasty Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 45 Abdominoplasty Kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1370-2017·2017-03-08

    Windstone Medical Spine Pack Gloves Recalled for Sterility Compromise

    Windstone Medical Packaging recalled 286 Spine Pack kits because the disposable gloves may contain splits or holes that compromise sterility.

    Product
    Spine Pack , part number AMS3753(A Spine Pack, part number AMS3783(A Spine Pack, part number AMS3783(B Spine Pack, part number AMS6472
    Category
    Medical Device
    Distribution
    26 states