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. 2,580 recalls have been distributed to Nebraska in the last 12 months.
Showing 12161–12180 of 49,150 recalls
Recalled Item: RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one...
The Issue: The outer package is mislabeled and the package contains a different IOL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...
The Issue: The affected staplers have the potential for the staple guide to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your 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: 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: 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: 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: 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) 5% 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) 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: Lidocaine 2% (20 mg/mL) Recalled by Olympia Compounding Pharmacy dba Olympia...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate 8.4% MDV Injection Recalled by Olympia Compounding...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T-106 Papaverine 30 mg/mL Phentolamine 1 mg/mL Alprostadil 25 mcg/mL...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Selenite 200 mg/mL Recalled by Olympia Compounding Pharmacy dba...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QM-4 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 300 mcg/mL...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.