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. 2,623 recalls have been distributed to Utah in the last 12 months.
Showing 10161–10180 of 28,579 recalls
Recalled Item: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valiant Navion Thoracic Stent Graft System. For endovascular repair of...
The Issue: Due to the presence of type IIIb endoleaks, stent fractures, and stent ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and...
The Issue: The tube holder can separate from the barrier that secures the device to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating Table System Recalled by Getinge Group Logistics America, LLC Due...
The Issue: There is a potential for hydraulic leakage at the inclination function to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosthesis Recalled by Howmedica Osteonics Corp. Due to Stryker has...
The Issue: Stryker has discovered that the internal profile of the Triathlon Tritanium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...
The Issue: This Field Action is being conducted following identification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A Recalled by...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan 3 mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Hypodermic Safety Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...
The Issue: Use of the kits after incorrect storage could lead to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...
The Issue: There is a potential that hand control units may cause the tabletop to slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 850 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000C Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000F Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination...
The Issue: Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000V Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Label - ACUSON Sequoia *** Power Input: 100-240V~ Recalled by...
The Issue: The ultrasound system averages the Mean Sac Diameter (MSD) and Gestational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack Infant Tubingset Pixie Flow 0 Recalled by Medtronic...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.