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.

51951–51975 of 78404

HighFDA (Food)·F-1403-2016·2016-06-01
Simply Delicious Recalls Lemon Poppyseed Oat Bars Due to Mispackaging
Simply Delicious is recalling Lemon Poppyseed Oat Bars because they were mispackaged with Coconut bars. The recall covers 142 cases distributed nationwide.
Product
Bobo's Oat Bars, Gluten Free, Lemon Poppyseed, Net Weight 3 oz (85g), packaged in clear plastic, 12 bars per sleeve, also sold as individual units. Manufactured by Simply Delicious, Inc.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1810-2016·2016-06-01
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 two boxes distributed worldwide.
Product
American Surgical Policot 1/2" x 2" Ref Number: 90-29 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1731-2016·2016-06-01
American Surgical Americot Blue Sponges Recalled for Packaging Defects
American Surgical Company is recalling Americot Blue sponges because defective packaging compromises sterility. The recall covers 24 boxes distributed worldwide.
Product
American Surgical Americot Blue 3/8" x 3/8" Ref Number: 20-22S Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1800-2016·2016-06-01
American Surgical Telfa Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Telfa neurosurgical sponges because defective packaging may compromise sterility.
Product
American Surgical Telfa 3/8" x 3" Ref Number: 80-05 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1798-2016·2016-06-01
American Surgical Uniqcot Sponges Recalled for Packaging Defect Compromising Sterility
American Surgical Company is recalling Uniqcot sponges because defective packaging may compromise sterility. The recall covers 3 boxes distributed worldwide.
Product
American Surgical Uniqcot 1/2" x 2" Ref Number: 67-29 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1764-2016·2016-06-01
American Surgical Ray-Cot Sponges Recalled for Packaging Sterility Defects
American Surgical Company is recalling Ray-Cot sponges because defective packaging may compromise sterility. The recall covers 165 boxes distributed worldwide.
Product
American Surgical Ray-Cot 1/4" x 1/4" Ref Number: 60-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1822-2016·2016-06-01
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 and lead to infection.
Product
Various trauma and sports medicine instruments and implants. Pin, fixation, smooth.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 97 boxes of Delicot 5 mm x 13 mm sponges because defective packaging may compromise sterility.
Product
American Surgical Delicot 5 mm x 13 mm Ref Number: 63-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1760-2016·2016-06-01
American Surgical Cotton Balls Recalled for Packaging Sterility Defect
American Surgical Company is recalling 10 boxes of non-strung cotton balls due to packaging defects that compromise sterility.
Product
American Surgical Cotton Balls-Non-Strung 3/4" Ref Number: 31-03 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1818-2016·2016-06-01
Biomet Recalls Arthroscopes and Implants Due to Sterile Seal Defects
Biomet is recalling various trauma and sports medicine instruments and arthroscopes because insufficient seal strength on sterile packaging could allow the product to become nonsterile.
Product
Various trauma and sports medicine instruments and implants. Arthroscope.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1740-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 22 boxes of Ultracot sponges because defective packaging may compromise sterility.
Product
American Surgical Ultracot 15 mm x 20 mm Ref Number: 23-04 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1775-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defects
American Surgical Company is recalling 287 boxes of Delicot sponges because defective packaging may compromise sterility.
Product
American Surgical Delicot 5 mm x 8 mm Ref Number: 63-01 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1762-2016·2016-06-01
American Surgical Cotton Balls Recalled Due to Packaging Sterility Defect
American Surgical Company is recalling 7 boxes of non-strung cotton balls due to packaging defects that compromise sterility. The affected lots were distributed worldwide.
Product
American Surgical Cotton Balls-Non-Strung 1/8" Ref Number: 31-07 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1724-2016·2016-06-01
American Surgical Americot Blue Sponges Recalled for Packaging Defect
American Surgical Company is recalling Americot Blue sponges because defective packaging may compromise sterility. The recall affects 262 boxes distributed worldwide.
Product
American Surgical Americot Blue 1/2" x 1/2" Ref Number: 20-04S Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1816-2016·2016-06-01
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 barrier packaging could compromise sterility and lead to infection.
Product
Various trauma and sports medicine instruments and implants. cannula, surgical, general & plastic surgery and accessories
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1723-2016·2016-06-01
American Surgical Sponges Recalled for Packaging Defect Compromising Sterility
American Surgical Company is recalling Americot Blue sponges because defective packaging may compromise sterility. The recall covers 54 cases distributed worldwide.
Product
American Surgical Americot Blue 1/4" x 1/4" Ref Number: 20-01S Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2016·2016-06-01
American Surgical Ray-Cot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Ray-Cot sponges because defective packaging may compromise sterility. The recall covers 209 boxes distributed worldwide.
Product
American Surgical Ray-Cot 1" x 3" Ref Number: 60-13 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1707-2016·2016-06-01
GE Healthcare Discovery IGS 740 Systems Recalled for Image Loss
GE Medical Systems is recalling 25 Discovery IGS 740 systems due to potential non-recoverable loss of image acquisition during procedures.
Product
GE Healthcare, Discovery IGS 740. Indicated for use in generating fluoroscopic and rotational images of human anatomy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2016·2016-06-01
American Surgical Delicot-J Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 27 boxes of Delicot-J sponges because defective packaging may compromise sterility.
Product
American Surgical Delicot-J 5 mm x 8 mm Ref Number: 63-01J (Japan Only) Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1748-2016·2016-06-01
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 products distributed in the US and 20 other countries.
Product
American Surgical Ultracot 30 mm x 70 mm Ref Number: 23-10 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1727-2016·2016-06-01
American Surgical Americot Blue Sponges Recalled for Packaging Defects
American Surgical Company is recalling 33 boxes of Americot Blue sponges because defective packaging may compromise sterility.
Product
American Surgical Americot Blue 1/2" x 3" Ref Number: 20-07S Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1737-2016·2016-06-01
American Surgical Ultracot Sponges Recalled for Packaging Defect Compromising Sterility
American Surgical Company is recalling 11 boxes of Ultracot sponges because defective packaging may compromise sterility. The products were distributed worldwide.
Product
American Surgical Ultracot 5 mm x 8 mm (Glassine) Ref Number: 23-01G Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0874-2016·2016-06-01
Akorn Recalls ORIS Chlorhexidine Oral Rinse Due to Impurity
Akorn, Inc. is recalling ORIS (chlorhexidine gluconate) oral rinse because multiple batches failed impurity specifications.
Product
ORIS (chlorhexidine gluconate), oral rinse, 0.12%, packaged in 16 fl. oz. (473 mL) PET bottle, Rx only, Manufactured for DENTSPLY Professional, York, PA 17404, UPC D00513003001O
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1797-2016·2016-06-01
American Surgical Uniqcot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling Uniqcot sponges because defective packaging may compromise sterility. The recall covers 15 cases distributed worldwide.
Product
American Surgical Uniqcot 1/2" x 3" Ref Number: 67-09 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1722-2016·2016-06-01
American Surgical Delicot Sponges Recalled for Packaging Sterility Defect
American Surgical Company is recalling 689 boxes of Delicot sponges because defective packaging may compromise sterility.
Product
American Surgical Delicot 30mm x 70mm Ref: 63-10 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide