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. 2,525 recalls have been distributed to West Virginia in the last 12 months.
Showing 8921–8940 of 27,884 recalls
Recalled Item: FIVE S 3.5x65 Recalled by Karl Storz Endoscopy Due to During a regular...
The Issue: During a regular requalification review, affected flexible intubation video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foundation Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare Due...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Pack Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenaculum Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endometrial Biopsy Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
The Issue: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) Recalled by Inpeco S.A. Due to The Firmware (FW) of the...
The Issue: The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoHelical and TomoDirect plans in RayStation 6 Recalled by RAYSEARCH...
The Issue: If the dynamic jaw mode is used and an optimization is continued after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee Recalled by...
The Issue: Packaging may include screws that are not intended to be used with the 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nexiva Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to...
The Issue: There is a breach in the product packaging that renders the product non-sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.