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 1321–1340 of 49,150 recalls

Medical DeviceSeptember 16, 2025· Medtronic Sofamor Danek USA Inc

Recalled Item: Catalyft PL & PL40 Expandable Interbody System labeled as follows Recalled...

The Issue: Expandable interbody system cage may loose height or collapse (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2025· Alcon Research LLC

Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
DrugSeptember 15, 2025· Graviti Pharmaceuticals Private Limited

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (XL) Recalled by...

The Issue: Failed Tablet/Capsule Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2025· Amerisource Health Services LLC

Recalled Item: Carbamazepine Extended-Release Tablets Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2025· Diagnostica Stago, Inc.

Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...

The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2025· Argon Medical Devices, Inc

Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...

The Issue: Due to complaints of increased resistance when advancing the dilator within...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2025· Philips North America

Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...

The Issue: Failure of Environmental Stress Testing from a pinched power module wire...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2025· Philips North America

Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...

The Issue: Failure of Environmental Stress Testing from a pinched power module wire...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: LGX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...

The Issue: The potential for devices to experience inflation and/or deflation...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
FoodSeptember 11, 2025· TROPICANA BRANDS GROUP

Recalled Item: Dole Apple Juice (primary package) Recalled by TROPICANA BRANDS GROUP Due to...

The Issue: A manufacturing process deviation occurred which may cause spoilage or...

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

Class II — Potential Health HazardOngoing
Refund