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. 2,439 recalls have been distributed to Nebraska in the last 12 months.
Showing 25981–26000 of 49,150 recalls
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Current Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...
The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura MP Recalled by St Jude Medical Inc. Due to The firm is...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor Recalled by St Jude...
The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model...
The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peaceful Mountain Recalled by Grato Holdings, Inc. Due to Multiple products...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peaceful Mountain -Stomach Rescue - Dietary supplement - Elemental silver...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...
The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...
The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.