The Recall Desk

State

Nebraska product recalls

73,817 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total
4,580
Critical
713
Severe
1,345
Most recent
2026-10-28

Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47326–47350 of 78397

  • 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
  • HighFDA (Devices)·Z-1284-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling Medtronic disposable gloves in custom kits because splits or holes may compromise sterility.

    Product
    Custom Pack, part number AMS4776 Custom Pack, part number AMS4776(A Custom Pack, part number AMS5643 Custom Pack, part number AMS5643(A Custom Pack, part number AMS6012 Custom Pack, part number AMS6383 Custom Pack, part number PSS2135(B Custom Pack, part number PSS2798(B…
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1319-2017·2017-03-08

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

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

    Product
    Hysteroscopy Pack, part number AMS4797 Hysteroscopy Pack, part number AMS4797(A Hysteroscopy Pack, part number AMS4797(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1364-2017·2017-03-08

    Windstone Medical Packaging Recalls Reduction Mammoplasty Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 35 Reduction Mammoplasty Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Reduction Mammoplasty Pack, part number AMS4380 Reduction Mammoplasty Pack, part number AMS4380(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1324-2017·2017-03-08

    Medtronic Gloves in AMS Lap Band Kits Recalled for Sterility Risk

    Windstone Medical Packaging is recalling 252 Lap Band kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Lap Band Pack, part number AMS1785(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1336-2017·2017-03-08

    Windstone Medical Recalls Lumbar Laminectomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 123 Lumbar Laminectomy Packs because the included gloves may have splits or holes that compromise sterility.

    Product
    Lumbar Laminectomy Pack, part number AMS2501 Lumbar Laminectomy Pack, part number AMS2501(A Lumbar Laminectomy Pack, part number AMS2501(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1345-2017·2017-03-08

    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
    Morris Hysto Pack, part number PSS3198(A
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1393-2017·2017-03-08

    Cook Inc. Recalls TriForce Peripheral Crossing Sets Due to Blood Loss Reports

    Cook Inc. is recalling 1,875 TriForce Peripheral Crossing Sets because a specific valve design is associated with increased reports of blood loss.

    Product
    TriForce Peripheral Crossing Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The TriForce Peripheral Crossing Set is intended to be percutaneously introduced into blood vessels and support a wire guide while performing percutaneous peripheral…
    Category
    Medical Device
    Distribution
    46 states
  • HighNHTSA·17V150000·2017-03-08

    Audi Recalls 2017 A5 and S5 Cabriolets for Seat Belt Pretensioner Defect

    Volkswagen Group of America is recalling 2017 Audi A5 and S5 Cabriolets because a seat belt pretensioner component may detach during a crash, creating a projectile hazard.

    Product
    AUDI — AUDI S5 CABRIOLET, A5 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2017·2017-03-08

    Windstone Medical Recalls Laparoscopic Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 1,056 Laparoscopic Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Laparoscopic Pack, part number AMS2499 Laparoscopic Pack, part number AMS2499(A Laparoscopic Pack, part number AMS2499(B
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1344-2017·2017-03-08

    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
    Minor/General/Ortho Pack, part number PSS3258(B
    Category
    Medical Device
    Distribution
    26 states