Product Recalls in Utah
Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,453 recalls have been distributed to Utah in the last 12 months.
Showing 27341–27360 of 49,677 recalls
Recalled Item: OptiView Amplification Kit (250 Test) Recalled by Ventana Medical Systems...
The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiView DAB IHC Detection Kit Recalled by Ventana Medical Systems Inc Due...
The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ultraView SISH Detection Kit Recalled by Ventana Medical Systems Inc Due to...
The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...
The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....
The Issue: Package integrity failure observed during routine shift package integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c5 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c5, Ampicilloyl were not met.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmunoCAP Allergen c6 Recalled by Phadia US Inc Due to The stability...
The Issue: The stability specifications of ImmunoCAP Allergen c6, Amoxicilloyl were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular E 170 Analyzer: Immunoassay Chemistry Analyzer Recalled by Roche...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...
The Issue: Presence of particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.