Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,415 recalls have been distributed to Wyoming in the last 12 months.
Showing 20781–20800 of 27,462 recalls
Recalled Item: Allura Xper FD20/20 OR Table Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optisure Dual Coil Defibrillation Leads Recalled by St Jude Medical Cardiac...
The Issue: Leads may have been compromised during the manufacturing process, with cuts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ FD OR table Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by Philips Electronics North...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/15 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS HM3000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...
The Issue: A component of the kit was found to contain bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted...
The Issue: The firm has received 15 complaints over ten years related to the connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Recalled by Insulet Corporation Due to Pod's needle mechanism fails...
The Issue: Pod's needle mechanism fails to deploy or there is a delay in the deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: Perfusion scan feature may not be available on machines running software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage System One S Cycler (High Permeability Hemodialysis System) Model...
The Issue: Ultrafiltration (UF) Volume software error inaccurate fluid removal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.