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. 1,850 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,850 in last 12 months

Showing 3414134160 of 53,829 recalls

Medical DeviceNovember 16, 2016· Teleflex Medical

Recalled Item: Weck Facial Closure Systems have application in laparoscopic procedures for...

The Issue: The devices wings may become partially detached from the EFx Shield during use.

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

Class II — Potential Health HazardOngoing
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C All Natural Parmesan/Romano Grated Cheese Recalled by 4 C Foods, Corp....

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C Homestyle All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp....

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to...

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C Homestyle All Natural Parmesan/Romano Grated Cheese Recalled by 4 C...

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C All Natural 100% Imported Italian Pecorino Romano Cheese Recalled by 4 C...

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: Cento Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: 4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese...

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: Cento Romano Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...

The Issue: FDA sample revealed the presence of Salmonella contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 15, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy 4 Implant Recalled by Implant Direct Sybron...

The Issue: The vial cap was mislabeled with the incorrect part number of 855708 but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: CARPAL TUNNEL PACK Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...

The Issue: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: SET UP PACK Surgical Instrument Tray Recalled by Robert Busse & Co. Inc....

The Issue: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: BREAST PACK Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...

The Issue: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Encore Medical, Lp

Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...

The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...

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

Class II — Potential Health HazardOngoing