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. 2,650 recalls have been distributed to Nebraska in the last 12 months.
Showing 1541–1560 of 49,150 recalls
Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Verio. Model Number: 10276755. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Lumina (DE). Model Number: 11344916. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396 Recalled by...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Vida Fit. Model Number: 11410481. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Cima.X (DE). Model Number: 11647158. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Verio Dot Upgrade. Model Number: 10684334. Recalled by Siemens...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Connectom.X. Model Number: 11371480. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Verio Dot. Model Number: 10684333. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extractor Pro RX Retrieval Balloon Catheter Recalled by Boston Scientific...
The Issue: The product in incorrectly labeled. The label indicates that the skive hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantiseptic Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other products and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KleenFoam Antimicrobial Foam Soap Recalled by DermaRite Industries, LLC Due...
The Issue: CGMP Deviation; manufactured at the same facility where other products and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermaFungal Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other products and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermaSarra Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other products and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PeriGiene Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other products and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermaMed Ointment Recalled by DermaRite Industries, LLC Due to CGMP...
The Issue: CGMP Deviation; manufactured at the same facility where other products and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PeriGuard Ointment Recalled by DermaRite Industries, LLC Due to CGMP...
The Issue: CGMP Deviation; manufactured at the same facility where other products and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.