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. 1,076 recalls have been distributed to Nebraska in the last 12 months.
Showing 12161–12180 of 49,150 recalls
Recalled Item: Morbillinum Recalled by Washington Homeopathic Products, Inc. Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tivicay (dolutegravir) Tablets 50 mg Recalled by GlaxoSmithKline LLC Due to...
The Issue: Labeling: incorrect or missing lot and/or expiration date. An incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Syphilinum Recalled by Washington Homeopathic Products, Inc. Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tuberculinum Recalled by Washington Homeopathic Products, Inc. Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Anagrelide Capsules USP Recalled by Teva Pharmaceuticals USA Inc Due to...
The Issue: Failed Dissolution Specifications- Low Out-Of-Specification results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Pill Splitters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product lid (which houses a blade) is coming unhinged from the base, thus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wise Woman Herbals Kava Capsules Recalled by EarthLab Inc Due to The...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wise Woman Herbals Standardized Kava Glycerite Recalled by EarthLab Inc Due...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...
The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE Recalled by...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE Recalled by...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) Recalled by Novartis...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% Recalled by Novartis...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CARESCAPE Central Station (CSCS) V2 Recalled by GE Healthcare, LLC Due to...
The Issue: The CARESAPE Central Station (CSCS) V2 can shut down due to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS) Recalled by Becton...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS) Recalled by...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.