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. 2,602 recalls have been distributed to Utah in the last 12 months.
Showing 10821–10840 of 28,579 recalls
Recalled Item: Philips Respironics V680 Ventilator Part Number 850011 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1137292 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number R1053618 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model...
The Issue: Potential for a false-negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva...
The Issue: Calibrator lots may not meet stability criteria and could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...
The Issue: Control lots may not meet stability criteria and could result in increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PryTime Medical - ER-Reboa Plus Catheter Recalled by Prytime Medical...
The Issue: There is a potential that catheters may have incorrectly marked balloon and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...
The Issue: Control lots may not meet stability criteria and could result in increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI Infusion Cannula 23G S - Product Usage: for use Recalled by Mani, Inc....
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G Recalled...
The Issue: The manufacturer has determined that with certain uncommon workflows there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. -...
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC VU360 Recalled by GE Healthcare, LLC Due to Incorrect patient...
The Issue: Incorrect patient identification and/or patient demographic errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults. When a 2D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in Recalled by...
The Issue: The firm has become aware of nine reports by a single customer that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.