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 1601–1620 of 49,150 recalls
Recalled Item: i-STAT EG7+ cartridge. List Number: 03P76-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz Recalled by...
The Issue: Mold. The firm noticed an increase in customer complaints. They conducted a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Northwind...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection 1000 mg/100 mL (10 mg/mL) Recalled by Baxter...
The Issue: Discoloration
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets USP Recalled by The Harvard Drug Group LLC dba Major...
The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MST ArcDUO 9mm Recalled by MicroSurgical Technology Inc Due to An ophthalmic...
The Issue: An ophthalmic knife has a suction set (not direct patient-contacting), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: READYPREP PVP Recalled by Medline Industries, LP Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Amneal...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringers's Injection USP Recalled by B BRAUN MEDICAL INC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Reviewed...
The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EverPatch+ Recalled by CORNEAT VISION, LTD. Due to Reviewed complaints have...
The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICEfx Cryoablation System Recalled by Boston Scientific Corporation Due to...
The Issue: Certain desiccant tube subassemblies were built with end caps that were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preventive Maintenance (PM) Kit ICEFX Recalled by Boston Scientific...
The Issue: Certain desiccant tube subassemblies were built with end caps that were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...
The Issue: Potential for activation of an abnormal alarm pause.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.