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. 2,650 recalls have been distributed to Nebraska in the last 12 months.
Showing 1701–1720 of 49,150 recalls
Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...
The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...
The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code:...
The Issue: As a result of Post-Market half-time stability testing, false negative test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000....
The Issue: Reports of out-of-box failures discovered during the limited launch phase....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019....
The Issue: Potential for undetected, deformed a-traumatic tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reef TA Inserter Recalled by SEASPINE ORTHOPEDICS CORPORATION Due to...
The Issue: Inserter, used as part of a system with an intervertebral body fusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...
The Issue: The catheters may not retain their shape.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...
The Issue: The catheters may not retain their shape.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...
The Issue: The catheters may not retain their shape.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensodyne PRONAMEL (Potassium nitrate 5% Recalled by Haleon US Holdings LLC...
The Issue: Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spironolactone Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Presence of foreign substance: identified as aluminum.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:slim X2 insulin pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Radiation Therapy Planning System: Multimodality Simulation...
The Issue: Due to a software issue, there is a potential image error of the Region of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number:...
The Issue: Packaging failures were identified which could lead to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Recalled by Integra...
The Issue: Packaging failures were identified which could lead to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.