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. 2,650 recalls have been distributed to Utah in the last 12 months.
Showing 3801–3820 of 28,579 recalls
Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-CR Model/Catalog Number: N/A...
The Issue: During positioning within the system's 3D to 3D matching mode while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to LIH Influence check...
The Issue: LIH Influence check settings for Lipemia are incorrect which may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cue Health COVID-19 Test Cartridge Cue COVID-19 Test Recalled by CUE HEALTH...
The Issue: Due to modified test kits being marketed and distributed without FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WOM Tube Set for lrrlgatlon Recalled by WOM World Of Medicine AG Due to...
The Issue: Incorrect transponder data was written on the RFID tags triggers the error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Image Guidance Functionality Recalled by Alcon Research LLC Due to...
The Issue: After surgery initiation, while using surgical image guidance, if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gray Revision Instrument System Accessory Tray/Case Recalled by Howmedica...
The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS Storage & Sterilization Case and Tray Recalled by Howmedica Osteonics...
The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: When a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: The reason for this recall is Beckman Coulter has determined that when a DxI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Infinity 5 Recalled by Abbott Medical Due to Their is a potential...
The Issue: Their is a potential that the implantable pulse generator replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Infinity 7 Recalled by Abbott Medical Due to Their is a potential...
The Issue: Their is a potential that the implantable pulse generator replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Infinity 5 Recalled by Abbott Medical Due to Their is a potential...
The Issue: Their is a potential that the implantable pulse generator replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Infinity 7 Recalled by Abbott Medical Due to Their is a potential...
The Issue: Their is a potential that the implantable pulse generator replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Model SL Tibial Components 16-2817/02 Tibial Component Recalled by...
The Issue: Blind screws of the modular tibial component cannot be loosened...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Model M Tibial Components Modular Knee Prosthesis System. Product...
The Issue: Blind screws of the modular tibial component cannot be loosened...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the...
The Issue: Potential for inaccurate fetal heart rate measurements when monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2nd Generation CentriMag Primary Console Recalled by Thoratec Switzerland...
The Issue: Due to a component change, the console part of a circulatory support system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Roadster Guide Sheath -PG4F90S -PG5F45MP -PG5F45R -PG5F45S Recalled...
The Issue: Due to older version of Instruction for Use (IFU) instructing to ensure that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Diluent Pack 3 Recalled by Ortho-Clinical...
The Issue: VITROS Chemistry Products FS Diluent Pack 3, Lot 01-1645 may cause results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System Manager Recalled by CareFusion 303, Inc. Due to Due to a...
The Issue: Due to a software issue the PC unit may not connect to the server which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.