Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,132 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,132 in last 12 months

Showing 1221–1240 of 49,150 recalls

Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: AFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator 9mm. Cranial Perforator. Recalled by Integra...

The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene...

The Issue: Zimmer Biomet is conducting a medical device recall for two (2) lots of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Collection Tube Extender Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: CARESCAPE ONE Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL MicroHematocrit Capillary Tubes Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: Portrait VSM Model nos. 6660000-666 Monitor Recalled by GE Healthcare...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 26, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Succinylcholine Chloride Injection Recalled by Dr. Reddy's Laboratories,...

The Issue: Out-of-Specification (OOS) result during the 6-month stability testing;...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator 11mm. Cranial Perforator. Recalled by Integra...

The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· DJO, LLC

Recalled Item: Cold Form Wrap: Back Recalled by DJO, LLC Due to The IFU (Information for...

The Issue: The IFU (Information for Use) on the wrap instructs the user to heat the hot...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 25, 2025· SV Labs Prescott Corporation

Recalled Item: Aloe Up Sport Performance Sunscreen Lotion SPF 30 Recalled by SV Labs...

The Issue: cGMP deviations: the firm released and distributed product which failed...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2025· Stryker Sustainability Solutions

Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...

The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 24, 2025· Now Foods

Recalled Item: NOW Real Food Organic Unsalted Whole Raw Cashews Recalled by Now Foods Due...

The Issue: Undeclared pine nut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...

The Issue: It was determined there is the potential of silicone fragments detaching...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing