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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2976129780 of 48,376 recalls

Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Integra LifeSciences Corp.

Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...

The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Merit Medical Systems, Inc.

Recalled Item: The PreludeSYNC Radial Compression Device is a sterile Recalled by Merit...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Eye Pad Oval Recalled by Covidien LLC Due to Product...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm) Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing