Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,943 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,943 in last 12 months

Showing 1914119160 of 29,425 recalls

Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Eye Pad Item Code: 03201 The sterile eye 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· 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· 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· Covidien LLC

Recalled Item: Covidien Curity Eye Pad Item Code: 91650 The sterile eye 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· 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 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
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