The Recall Desk

State

Georgia product recalls

73,824 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,635
Critical
1,471
Severe
2,567
Most recent
2026-11-04

Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.

These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50476–50500 of 83459

  • HighFDA (Devices)·Z-1392-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Introducer Devices Due to Blood Loss Reports

    Cook Inc. is recalling 29 Check-Flo Introducer Hausdorf-Lock Atrial devices worldwide due to increased reports of blood loss associated with the hemostatic valve design.

    Product
    Check-Flo Introducer Hausdorf-Lock Atrial, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1276-2017·2017-03-08

    Windstone Medical Packaging Recalls Breast Augmentation Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 1,436 breast augmentation kits because the disposable gloves included may contain splits or holes that compromise sterility.

    Product
    Breast Augmentation Pack, part number AMS1786(A Breast Augmentation Pack, part number AMS2790(A Breast Augmentation Pack, part number AMS3324(B Breast Augmentation Pack, part number AMS4382 Breast Augmentation Pack, part number AMS4382(A Breast Augmentation Pack, part…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1291-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits because splits or holes may compromise sterility.

    Product
    Dr. Casey Pack, part number AMS4313(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1389-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Hemostasis Assemblies Due to Blood Loss Reports

    Cook Inc. is recalling 1,589 Check-Flo Hemostasis Assemblies because reports indicate increased blood loss associated with the device's valve design.

    Product
    Check-Flo Hemostasis Assembly, Individual product is packaged in a Tyvek-film sterilizable outer pouch.
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1264-2017·2017-03-08

    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
    Basic Extended Pack, part number AMS4421(A Basic Extended Pack, part number AMS4421(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1311-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Sterility Compromise

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

    Product
    Hand Pack, part number AMS3640 Hand Pack, part number AMS4213(A Hand Pack, part number AMS4311(A Hand Pack, part number AMS5343 Hand Pack., part number PSS1843(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1259-2017·2017-03-08

    Medtronic Gloves in AMS Kits Recalled for Sterility Compromise

    Windstone Medical Packaging is recalling 174 Angio Pack kits because the Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Angio Pack, part number AMS6711
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1266-2017·2017-03-08

    Windstone Medical Packaging Recalls Basic Kits with Defective Gloves

    Windstone Medical Packaging is recalling 216 Basic Kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Basic Kit, part number CMP1109(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1356-2017·2017-03-08

    Windstone Medical Recalls Pacemaker Kits Due to Sterility Compromise

    Windstone Medical Packaging is recalling 561 pacemaker kits because the disposable gloves included may contain splits or holes that compromise sterility.

    Product
    Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1387-2017·2017-03-08

    Cook Inc. Recalls Check-Flo Performer Introducers Due to Blood Loss Reports

    Cook Inc. is recalling 884 Check-Flo Performer Introducers because a specific valve design is associated with increased reports of blood loss.

    Product
    Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1315-2017·2017-03-08

    Windstone Medical Recalls Hernia Packs with Defective Gloves

    Windstone Medical Packaging is recalling 228 Hernia Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Hernia Pack, part number AMS3859
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1292-2017·2017-03-08

    Windstone Medical Recalls Dr. Landi EVLT Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 944 Dr. Landi EVLT Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Dr. Landi EVLT Pack, part number AMS1483(E Dr. Landi EVLT Pack, part number AMS1483(E
    Category
    Medical Device
    Distribution
    26 states