The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

33101–33125 of 50502

  • HighFDA (Devices)·Z-1360-2017·2017-03-08

    Medtronic 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
    Plastic Kit, part number CMP1084(C
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1326-2017·2017-03-08

    Windstone Medical Recalls Lap Gallbladder Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 225 Lap Gallbladder Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Lap Gallbladder Pack, part number AMS3707
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1378-2017·2017-03-08

    Medtronic Gloves in AMS Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 1,787 Upper Extremity Packs because the Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Upper Extremity Pack, part number AMS4670 Upper Extremity Pack, part number AMS4670(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1290-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

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

    Product
    Dr Bragg Vein Tray - RX, part number 007912-8
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1285-2017·2017-03-08

    Windstone Medical Packaging Recalls Custom Kits with Defective Gloves

    Windstone Medical Packaging is recalling 840 custom kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Custom Pack - with Introducer Kit, part number TVS4011NI(L
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1346-2017·2017-03-08

    Windstone Medical Recalls Morris Lap Packs Due to Sterility Compromise

    Windstone Medical Packaging is recalling Morris Lap Packs because the disposable gloves included in the kits may contain splits or holes that compromise sterility.

    Product
    Morris Lap Pack, part number PSS3199(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1320-2017·2017-03-08

    Windstone Medical Recalls Knee Arthroscopy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 700 knee arthroscopy packs because the disposable gloves included may have splits or holes that compromise sterility.

    Product
    Knee Arthroscopy Pack , part number AMS2610(A Knee Arthroscopy Pack, part number AMS3236(A Knee Arthroscopy Pack, part numbre AMS3860
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1297-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

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

    Product
    Extremity Pack-N Brunswick, part number PSS1866(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1277-2017·2017-03-08

    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
    Breast Pack, part number AMS3238(A Breast Pack, part number AMS4419(A Breast Pack, part number AMS4419(B Breast Pack, part number AMS5750 Breast Pack, part number AMS5750(A Breast Pack, part number AMS6120 Breast Pack, part number PSS1784(B Breast Pack, part number…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1269-2017·2017-03-08

    Medtronic Gloves in AMS Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 276 Basic Setup Packs because the Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Basic Setup Pack, part number AMS1787(A Basic Setup Pack, part number AMS6519
    Category
    Medical Device
    Distribution
    26 states
  • HighNHTSA·17V148000·2017-03-07

    Mercedes-Benz Metris Recall for Non-Functioning Blind Spot Monitoring

    Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Metris vans because the Blind Spot Monitoring system does not work due to incompatible parts.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E014000·2017-03-07

    H&H Sports Protection Recalls TORC T-55 V2 Motorcycle Helmets

    H&H Sports Protection is recalling TORC T-55 V2 half helmets because they may not adequately protect the wearer or stay secured during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17733·2017-03-07

    L.L. Bean Recalls Snowshoes Due to Plastic Frame Breakage Hazard

    L.L. Bean is recalling Adventure Adjustable Snowshoes because the plastic deck can weaken and break, posing a fall hazard. No injuries have been reported.

    Product
    Snowshoes and snowshoe packages
    Category
    Consumer Product
    Distribution
    Distributed nationwide