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. 1,132 recalls have been distributed to Nebraska in the last 12 months.
Showing 1521–1540 of 49,150 recalls
Recalled Item: Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX...
The Issue: To provide further information to the user to ensure proper use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM Solution Set Recalled by Baxter Healthcare Corporation Due...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bevacizumab (Avastin) Injection Recalled by Fagron Compounding Services Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sharesource Connectivity Platform for Use with Homechoice Claria Product...
The Issue: Vantive has identified a software defect within the Sharesource Claria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Prisma. Model Number: 10849582. 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 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 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: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...
The Issue: Failed Impurities/Degradation Specifications:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...
The Issue: Failed Impurities/Degradation Specifications:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biograph mMR. Model Number: 10433372. Recalled by Siemens Medical Solutions...
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: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...
The Issue: Failed Impurities/Degradation Specifications:
Recommended Action: Stop taking this medication. Contact your pharmacy or 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.