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. 2,471 recalls have been distributed to Utah in the last 12 months.
Showing 23681–23700 of 28,579 recalls
Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by...
The Issue: It was determined that a defective sieve bed subassembly enabled zeolite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...
The Issue: There is a potential for unintended and erratic motion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: MaxLock Extreme Mod-Foot Concave Reamer Recalled by Orthohelix Surgical...
The Issue: Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...
The Issue: Customer complaints were received for positive bias reported on the controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...
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: External power supply adaptors that accompany Clinitek Status+ The Clinitek...
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: 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: 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: 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 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: 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: 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: 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 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: 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: 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: 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.