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. 2,537 recalls have been distributed to West Virginia in the last 12 months.
Showing 5521–5540 of 27,884 recalls
Recalled Item: EVIS EXERA III Video System Center Model Number CV-190. Intended Recalled by...
The Issue: Certain serial numbers of the CV-190 do not start up properly because parts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Acrobat-i Vacuum Stabilizer System Intended for use during...
The Issue: Housing Mount Jaw of these devices breaking during normal use and may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 and Astral 150 ventilators Recalled by ResMed Ltd. Due to If...
The Issue: If ventilator is on internal battery, not intended to serve as a primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...
The Issue: Syringe contains conical tip that is not compatible with certain needleless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
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: The firm has investigated and confirmed that when DxI 9000 is connected to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...
The Issue: Thunderbeats blue seal button may remain in the engaged position after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System Recalled by...
The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Plus Aerobic/F Culture Vials Recalled by Becton Dickinson & Co....
The Issue: Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sapphire Infusion Pumps Recalled by EITAN MEDICAL LTD Due to Infusion Pumps...
The Issue: Infusion Pumps with affected software revision may fail to detect air in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.