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. 2,400 recalls have been distributed to Nebraska in the last 12 months.
Showing 38701–38720 of 49,150 recalls
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to CGMP...
The Issue: CGMP Deviations: Product excipient was not re-tested at the appropriate date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mafenide Acetate Recalled by Par Pharmaceutical Inc. Due to Presence of...
The Issue: Presence of Foreign Substance; oxidized steel, organic material and shredded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...
The Issue: Devices were not sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging Recalled...
The Issue: Devices were not sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon...
The Issue: Potential for weld disassociation of the cross pin, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...
The Issue: A false negative result affecting the diagnosis may occur. A defect in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic Sacha Inchi Powder Recalled by Sunfood Corportation Due to Sunfood...
The Issue: Sunfood is recalling Sacha Inchi Powder because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...
The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...
The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...
The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...
The Issue: Incorrect size printed on the Milex Pessary Kit packaging label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200...
The Issue: Microbial Contamination of Non-Sterile Products: Lots failed microbiological...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.