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. 2,450 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,450 in last 12 months

Showing 1830118320 of 27,884 recalls

Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: HYFRECATOR 2000 HANDPIECE SHEATH Recalled by ConMed Corporation Due to For...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx50cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental vss bowed 19x190mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx46cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx42cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 14mmdx50cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Xl por st 25.5x220mm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 20x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· ConMed Corporation

Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...

The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Stryker Communications

Recalled Item: The Stryker Visum¿ LED Surgical Lighting system is intended to Recalled by...

The Issue: The potential hazard that can arise for the combination of the missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 17x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx50cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 18x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing