Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,393 recalls have been distributed to West Virginia in the last 12 months.
Showing 21561–21580 of 27,884 recalls
Recalled Item: Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L Recalled...
The Issue: The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC Recalled...
The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc....
The Issue: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abutment Retrieval Instrument Zirconia CC RP/WP Recalled by Nobel Biocare...
The Issue: One dimension of the affected instrument is incorrect. Therefore this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...
The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to the...
The Issue: the Fabius MRI or parts of the system were attracted by the magnetic field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Recalled...
The Issue: Incorrect expiration date on outer carton kit label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Recalled by Acon...
The Issue: Acon Laboratories, Inc. is recalling Mission Breath Alcohol Detector due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Expression MRI Patient Monitoring System. Recalled by Philips...
The Issue: The device's labeling inaccurately indicates Endotracheal as a body...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTRUMENT ARM DRAPE Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field Safety Notification to advise of an issue that may occur involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable...
The Issue: The Supporter toilet armrest has two Fast Nuts fixing the product to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPD-Scan III Power/Corneal Analyzer Opthalmic Software versions 1.00.08...
The Issue: Software bug was found where there was no difference in Total and Corneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-Stat PT/INR Cartridges List number 03P89-24 The cartridges are packaged...
The Issue: Certain lots of PT/INR cartridges may generate a higher than typical number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Block Versions Used by Dental Offices often to as Recalled by 3M Company -...
The Issue: 3M is initiating a Field Correction to remove the crown indication from all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Potential colonization of organisms, including Mycobacteria, in Sorin Heater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.