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. 2,450 recalls have been distributed to Utah in the last 12 months.
Showing 31901–31920 of 49,677 recalls
Recalled Item: Monaco RTP System Recalled by Elekta, Inc. Due to Incorrect Dose when using...
The Issue: Incorrect Dose when using the reset function.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOCO Futurabond M+ adhesive Recalled by Voco GmbH Due to Labeling mix-up:...
The Issue: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue where certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Cable WA00014A Recalled by Olympus Corporation of the Americas Due to...
The Issue: Software malfunction that results in incorrect generation or display of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Zydus...
The Issue: Failed Dissolution Specifications; 6 month time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Complaints of broken tips on the ampules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 40 Mcg Recalled by Teva...
The Issue: Failed Content Uniformity: Product was out of specification for spray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg Recalled by Teva...
The Issue: Failed Content Uniformity: Product was out of specification for spray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AXIOM Artis Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile...
The Issue: Package may be incorrectly labeled as containing 0.76 mm Drill Bit, but in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC unit Recalled by CareFusion 303, Inc. Due to Reports where...
The Issue: Reports where the Low Battery alarm and/or the Very Low Battery alarm are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA Recalled by Owens...
The Issue: Owens & Minor is the initial importer and private label distributor of Medi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy Recalled by Mevion...
The Issue: Completing Setup Without Program Move Complete Can Cause An Isocenter Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Elite Atherectomy Catheter. Models: 410-152 Recalled by Spectranetics...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.