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. 2,460 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,460 in last 12 months

Showing 1690116920 of 27,884 recalls

Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing