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. 1,069 recalls have been distributed to Nebraska in the last 12 months.
Showing 14201–14220 of 49,150 recalls
Recalled Item: Artis Q.zen ceiling with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q biplane with software VD12-angiography systems developed for single...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspiration Syringe Kit Recalled by MICROVENTION INC. Due to Syringe Kits...
The Issue: Syringe Kits labeled for distribution OUS were inadvertently shipped to US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gatifloxacin Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Failed Stability Specifications: Out-of-specification results observed in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Whole raw WHITE onions are imported from Chihuahua of MEXICO. Recalled by...
The Issue: Salmonella Oranienburg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole raw RED onions are imported from Chihuahua of MEXICO. Recalled by...
The Issue: Salmonella Oranienburg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole raw YELLOW onions are imported from Chihuahua of MEXICO. Recalled by...
The Issue: Salmonella Oranienburg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Model B35200 - Percept PC BrainSense Implantable Neurostimulator Recalled by...
The Issue: During cardioversion events, the Model B35200 Percept PC Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nimbus PainPro Ambulatory Infusion Pumps with software version v4 Recalled...
The Issue: An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cubicin (daptomycin for injection) Recalled by MERCK SHARP & DOHME CORP Due...
The Issue: Presence of Particulate Matter: Identified as Glass Particles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 5mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 10mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Film Coated Tablets Recalled by MACLEODS PHARMA USA,...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cobas u 601 urinalysis test system Recalled by Roche Diagnostics Operations,...
The Issue: A potential risk for false negative nitrite results exists when endogenous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Udel Sterilization Tray Instructions for Use Recalled by Karl...
The Issue: To ensure sterilization effectiveness, sterilization tray instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...
The Issue: During stent graft deployment, the spindle may detach from the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...
The Issue: There is a potential to display incomplete patient imaging study.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.