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. 2,397 recalls have been distributed to Utah in the last 12 months.
Showing 41181–41200 of 49,677 recalls
Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has recently become aware of a potential safety issue to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z- GAS II EFFERVESCENT GRANULES Antacid/Antiflatulent Recalled by Bracco...
The Issue: Subpotent Drug: Out of Specification (OOS) result during routine stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiopulmonary bypass connector Recalled by Dokitz NovoSci Due to The...
The Issue: The single leg of the PAY connector has been observed to become detached.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 instrument for the da Vinci Si System Recalled by...
The Issue: Intuitive is issuing an urgent product notice to all users of the EndoWrist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice¿ Multifunction Electrode Part Number: MC171 OH Recalled by...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A Recalled...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xarelto (rivaroxaban) Tablets 15 mg per tablet Recalled by Janssen Ortho...
The Issue: Microbial Contamination of Non-Sterile Products: Consumer complaint...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ProClear Toric contact lenses are made from a material containing Recalled...
The Issue: Routine quality monitoring system has identified that a limited number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to...
The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...
The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer used in conjunction with the da Recalled by...
The Issue: Intuitive Surgical is initiating a voluntary correction relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Prefilled Buffered 10% Formalin. Product Usage:10% NBF is...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard-Allan Scientific Specimen Transportation System. Product Usage: 10%...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protocol 10% NBF Product Usage: 10% NBF is used to Recalled by Richard-Allan...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard-Allan Scientific Bio-Tite Specimen Containers. Product Usage: 10%...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.