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. 2,466 recalls have been distributed to Utah in the last 12 months.
Showing 24801–24820 of 28,579 recalls
Recalled Item: Symbia T and Symbia T2 computer tomography systems. These systems Recalled...
The Issue: There are confirmed reports of a component coming loose inside the CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....
The Issue: The outer package label contained the incorrect length of the device. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...
The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM 6 Monitor in use with a Multi Parameter Module Recalled by Mindray DS...
The Issue: The MPM included a cardiac ST/Arrhythmia analysis feature which is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down....
The Issue: Remington Medical discovered an error on the FL-601-97 IFU; part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800...
The Issue: Sterility of the product cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II Implant Kit with Pocket Controller Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Mate II Pocket Controllers removed from packaging Product Usage:...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer Recalled by Roche...
The Issue: electrode used beyond the guaranteed in-use 52 week lifetime,may leak and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...
The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...
The Issue: GE Healthcare has recently become aware of potential safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.