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.

Which agencies issued them

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.

47376–47400 of 78397

  • 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-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
  • HighFDA (Devices)·Z-1341-2017·2017-03-08

    Windstone Medical Minor Packs Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling 665 Minor Packs because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Minor Pack, part number AMS3782(B Minor Pack, part number AMS3782(C Minor Pack, part number CMP1560 Minor Pack, part number PSS3518(B Minor Pack, part number PSS3541(A
    Category
    Medical Device
    Distribution
    26 states
  • 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