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 2321–2340 of 49,150 recalls
Recalled Item: Semaglutide Recalled by Thrive Health and Wellness, LLC, dba Thrive Health...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CJC-1295 Injectable Recalled by Thrive Health and Wellness, LLC, dba Thrive...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LX Bioboost Plus Recalled by Thrive Health and Wellness, LLC, dba Thrive...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LL Bioboost Injectable Recalled by Thrive Health and Wellness, LLC, dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide/Cyanocobalamin Injectable Recalled by Thrive Health and...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tirzepatide Injections Recalled by Thrive Health and Wellness, LLC, dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotinamide adenine dinucleotide (NAD+): 100mg/mL Recalled by Thrive Health...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UNAVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients
The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UMOVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients
The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen...
The Issue: Due to a software/firmware issue diabetes management system may provide a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...
The Issue: Due to demonstration units of chest compression system being provided to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.