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.

48,376 total recalls
2,393 in last 12 months

Showing 2170121720 of 27,884 recalls

Medical DeviceMay 28, 2015· Synthes, Inc.

Recalled Item: Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts Recalled by Synthes,...

The Issue: It was reported that the RIA Drive Shaft, Tube Assembly, and Reamer Head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· Synthes, Inc.

Recalled Item: Pull Reduction Device For 4.3mm Percutaneous Drill Guide Recalled by...

The Issue: Certain affected parts and lots of the Pull Reduction Devices may have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· Cook Inc.

Recalled Item: Ring Transjugular Intrahepatic Access Set Product Usage: The Ring...

The Issue: Cook Inc. is initiating a voluntary recall of the Ring Transjugular...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: 365¿M Lithotripsy Fiber- Reusable Recalled by American Medical Systems...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: 1X1 Cleaving Tiles Recalled by American Medical Systems Innovation Center -...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Sureflex 273 Lithotripsy Fiber Recalled by American Medical Systems...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: 200¿M Lithotripsy Fiber- Reusable Recalled by American Medical Systems...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· Cook Inc.

Recalled Item: Flexor RTPS Guiding Sheath Product Usage: The Flexor RTPS Guiding Recalled...

The Issue: Cook Inc. is initiating a voluntary recall of the Ring Transjugular...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2015· American Medical Systems Innovation Center - Silicon Valley

Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...

The Issue: validation data related to cleaning instructions and sterilization methods...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Allofix Insertion Kit Recalled by Musculoskeletal Transplant Foundation,...

The Issue: Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG (TPS) Stylet 5F Maximal Recalled...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Integra LifeSciences Corp.

Recalled Item: Integra Camino Intracranial Pressure Monitoring Catheter with Licox IMC Bolt...

The Issue: Integra LifeSciences is recalling the Camino Intracranial Pressure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Sherlock 3CG TPS Stylet 4F Maximal Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2015· Synthes, Inc.

Recalled Item: DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm Recalled by...

The Issue: certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2015· Bard Access Systems

Recalled Item: PowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Recalled by...

The Issue: Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing