State

Nebraska product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51876–51900 of 78404

HighFDA (Devices)·Z-1812-2016·2016-06-01
Draeger D-Vapor Anesthesia Vaporizers Recalled for Anesthetic Agent Release
Draeger Medical is recalling D-Vapor and D-Vapor 3000 anesthesia vaporizers because they may release desflurane during filling, posing an eye irritation risk.
Product
Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and Bottles. Catalog # M35500 (D-Vapor) and M36700 (D-Vapor 3000). Anesthesia Vaporizer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Defect Compromising Sterility
American Surgical Company is recalling 33 boxes of Ultracot sponges because defective packaging may compromise sterility. The affected products were distributed worldwide.
Product
American Surgical Ultracot 30 mm x 90 mm (Glassine) Ref Number: 23-15G Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1799-2016·2016-06-01
American Surgical Cylindrical Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 11 boxes of cylindrical sponges because defective packaging may compromise sterility.
Product
American Surgical Cylindrical Sponges-Strung 1/2" x 1.5" Ref Number: 70-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1809-2016·2016-06-01
American Surgical Policot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Policot sponges because defective packaging compromises sterility. The products were distributed worldwide.
Product
American Surgical Policot 1/2" x 1.5" Ref Number: 90-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2016·2016-06-01
American Surgical Telfa Sponges Recalled for Packaging Sterility Defects
American Surgical Company is recalling Telfa 1/2" x 1/2" sponges because defective packaging may compromise sterility. The recall covers 24 boxes distributed worldwide.
Product
American Surgical Telfa 1/2" x 1/2" Ref Number: 80-06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1750-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Ultracot sponges because defective packaging may compromise sterility. The recall covers 6 boxes distributed worldwide.
Product
American Surgical Ultracot 15 mm x 15 mm (Glassine) Ref Number: 23-12G Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1808-2016·2016-06-01
American Surgical Policot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Policot sponges because defective packaging may compromise sterility. The products were distributed worldwide.
Product
American Surgical Policot 1/2" x 1/2" Ref Number: 90-06 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1781-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Compromise
American Surgical Company is recalling Delicot non-xray sponges because defective packaging compromises sterility. The recall covers 4 boxes distributed worldwide.
Product
American Surgical Delicot non-xray 10 mm x 13 mm Ref Number: 63-03 non-xray Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1739-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 41 boxes of Ultracot sponges because defective packaging may compromise sterility.
Product
American Surgical Ultracot 10 mm x 13 mm (Glassine) Ref Number: 23-03G Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2016·2016-06-01
American Surgical Ray-Cot Sponges Recalled for Sterility Compromise
American Surgical Company is recalling Ray-Cot sponges because defective packaging may have compromised sterility. The recall covers 28 boxes distributed worldwide.
Product
American Surgical Ray-Cot 1/2" x 1.5" Ref Number: 60-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1828-2016·2016-06-01
Biomet Recalls Trauma and Sports Medicine Implants Due to Seal Defects
Biomet is recalling various trauma and sports medicine instruments and implants because insufficient seal strength on sterile packaging could compromise sterility and lead to infection.
Product
Various trauma and sports medicine instruments and implants. Fastener, fixation, nondegradable, soft tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1761-2016·2016-06-01
American Surgical Cotton Balls Recalled for Packaging Sterility Defects
American Surgical Company is recalling 3 boxes of 1-inch non-strung cotton balls due to packaging defects that compromise sterility.
Product
American Surgical Cotton Balls-Non-Strung 1" Ref Number: 31-04 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1770-2016·2016-06-01
American Surgical Ray-Cot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 102 boxes of Ray-Cot 1" x 1" sponges because defective packaging compromises sterility.
Product
American Surgical Ray-Cot 1" x 1" Ref Number: 60-12 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1757-2016·2016-06-01
American Surgical Cotton Balls Recalled for Packaging Sterility Defects
American Surgical Company is recalling 237 units of 1-inch strung cotton balls due to packaging defects that compromise sterility.
Product
American Surgical Cotton Balls-Strung 1" Ref Number: 30-04 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1736-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 114 cases of Ultracot sponges because defective packaging compromises sterility.
Product
American Surgical Ultracot 5 mm x 8 mm Ref Number: 23-01 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1820-2016·2016-06-01
Biomet Recalls Trauma and Sports Medicine Instruments Due to Seal Defects
Biomet is recalling various trauma and sports medicine instruments and implants because insufficient seal strength on sterile packaging could compromise sterility.
Product
Various trauma and sports medicine instruments and implants. Reamer.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V390000·2016-06-01
Pierce Emergency Vehicles Recalled for Improperly Soldered Pump Strainers
Pierce is recalling 2015-2016 emergency vehicles because pump intake strainers may be improperly soldered, risking pump damage and reduced firefighting effectiveness.
Product
PIERCE — PIERCE VELOCITY, ARROW XT, SABER, IMPEL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1779-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 21 boxes of Delicot non-xray sponges because defective packaging may compromise sterility.
Product
American Surgical Delicot non-xray 5 mm x 13 mm Ref Number: 63-02 non-xray Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1787-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defects
American Surgical Company is recalling 409 boxes of Delicot sponges because defective packaging may compromise sterility.
Product
American Surgical Delicot 13 mm x 60 mm Ref Number: 63-08 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1826-2016·2016-06-01
Biomet Recalls Trauma and Spinal Implants Due to Sterile Seal Defects
Biomet is recalling various trauma, sports medicine, and spinal implants because insufficient seal strength may compromise sterility, potentially leading to infection.
Product
Various trauma and sports medicine instruments and implants. Spinal interlaminal fixation orthosis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1811-2016·2016-06-01
American Surgical Company Recalls Neurosurgical Sponges Due to Packaging Defect
American Surgical Company is recalling 16 boxes of Mass Eye & Ear Finger Cot Nasal sponges because defective packaging compromises sterility.
Product
Mass Eye & Ear Finger Cot Nasal 2's Ref Number: 41-04 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1784-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Defect Compromising Sterility
American Surgical Company is recalling 99 units of Delicot 4 mm x 50 mm sponges because defective packaging may compromise sterility.
Product
American Surgical Delicot 4 mm x 50 mm Ref Number: 63-05 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 27 boxes of Ultracot sponges because defective packaging may compromise sterility. The products were distributed worldwide.
Product
American Surgical Ultracot 70 mm x 10090 mm Ref Number: 23-24 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1824-2016·2016-06-01
Biomet Recalls Trauma and Sports Medicine Instruments Due to Seal Defects
Biomet, Inc. is recalling various trauma and sports medicine instruments and implants because insufficient seal strength on sterile packaging could compromise sterility and lead to infection.
Product
Various trauma and sports medicine instruments and implants. Passer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1807-2016·2016-06-01
American Surgical Policot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Policot sponges because defective packaging may compromise sterility. The recall covers 3 boxes distributed worldwide.
Product
American Surgical Policot 1/4" x 1/4" Ref Number: 90-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide