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 28221–28240 of 28,579 recalls
Recalled Item: Toshiba Ultra-Short Magnetic Resonance Imaging System Recalled by Toshiba...
The Issue: The firm recalled due to a potentail problem with the position of the hold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW-I Anesthesia System The system is intended for use in Recalled by...
The Issue: A technical alarm may be generated on the FLOW-i system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow IV Fluid Warmer (510k name: EFLOW IV FLUID WARMER Recalled by Vital...
The Issue: The EnFlow Warmer Strap does not meet the requirements of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module with v2.0 software used Recalled...
The Issue: GE Healthcare became aware of two issues with the Patient Data Module using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle Recalled by...
The Issue: A Discrepancy was found on Hitachi AST (HA7 61) package insert. Limitations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Advansys Medial Lisfranc Plate (MLP) Recalled by Integra...
The Issue: Incorrect technique applied may cause potential rupture of the tibialis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The finger cots are made out of natural rubber. They Recalled by Afassco Inc...
The Issue: The firm is initiating a field correction because the product(s) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CaviCide Recalled by Metrex Research, LLC. Due to Metrex Research is...
The Issue: Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump System Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.