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. 2,612 recalls have been distributed to Nebraska in the last 12 months.
Showing 7901–7920 of 28,140 recalls
Recalled Item: The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit...
The Issue: Due to preventative maintenance (PM) not being performed on E-100 generators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to When a run is aborted,...
The Issue: When a run is aborted, the cooling period protection does not occur and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Monitor Recalled by Integra LifeSciences Corp. Due to Integra...
The Issue: Integra has received complaints associated with ICP readings drifting to -50...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Cholesterol- For the quantitative in vitro determination of...
The Issue: Product fails to meet the performance claims quoted on the kit insert:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...
The Issue: Device was marketed without FDA 510(k) clearance or a PMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit...
The Issue: BD Intraosseous Needle Kits may exhibit: 1) Increased force required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene CDF Nucleic Acid Test Recalled by Luminex Corporation Due to There...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER37000 programmer Model MER3400 software Recalled by St. Jude...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: There is a potential for programmer software (Merlin PCS) and remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin.net model MN5000 Software Recalled by St. Jude Medical, Cardiac...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Enteric Pathogens Nucleic Acid Test Recalled by Luminex Corporation...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various ob/gyn packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Angiography packs/trays Recalled by American Contract Systems, Inc....
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breast Abdominoplasty Pack Recalled by American Contract Systems, Inc. Due...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various C-section packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various convenience packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various convenience packs Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D&C pack Recalled by American Contract Systems, Inc. Due to Product was...
The Issue: Product was exposed to multiple sterilization cycles without validation for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.