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. 2,466 recalls have been distributed to Nebraska in the last 12 months.
Showing 21641–21660 of 49,150 recalls
Recalled Item: Norm-O-Temp model 111W Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios care fusion system Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: DAP chamber may be missing an insulating foil
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha VA20/ VA30 mobile X-Ray systems Recalled by Siemens Medical...
The Issue: DAP chamber may be missing an insulating foil
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROXOCOBALAMIN 1000 MCG/ML (MDV) Recalled by RXQ Compounding LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETAMINE 10 MG/ML INJ SOL SYR (C-III) Recalled by RXQ Compounding LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TURBO CAINE 2.5 (PHEN2.5/CYCLO1/ TROP1/TETRA 0.5) Recalled by RXQ...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLUTATHIONE 200MG/ML (MDV) INJECTION SOLN Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITAMIN B COMPLEX 100 (MDV) Recalled by RXQ Compounding LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORPHINE 1MG/ML IN NACL 0.9% 55ML SYR (C-II) Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRAVASOL 10% (AMINO ACID) INJECTION SOLUTION Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUFFERED LIDOCAINE HCL 1% INJECTION SOL (PF) SYR Recalled by RXQ Compounding...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROMORPHONE 0.2MG/ML IN NACL 0.9% SYR (C-II) Recalled by RXQ Compounding...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ONDANSETRON 2 MG/ML INJECTION SOLUTION (PFV) Recalled by RXQ Compounding LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.