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. 1,849 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,849 in last 12 months

Showing 3618136200 of 53,829 recalls

FoodMay 23, 2016· Let's Do Lunch, Inc.

Recalled Item: Integrated Food Service Submarine on a French Roll Turkey Bolo Recalled by...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2016· Let's Do Lunch, Inc.

Recalled Item: Integrated Food Service Chicken Patty Sandwich Chicken Patty on a Recalled...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2016· Coca-Cola Company (The)

Recalled Item: Honest Kids-Super Fruit Punch Recalled by Coca-Cola Company (The) Due to The...

The Issue: The label does not list apple juice ingredient present in the beverage.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 23, 2016· Steris Corporation

Recalled Item: OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due...

The Issue: STERIS has identified that the pivot pin assembly located on the table top...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Proximal Foot/Left Recalled by Synthes (USA)...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Left Foot/20mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Right Foot/20mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Proximal Foot/Right Recalled by Synthes (USA)...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Right Foot/30mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Synthes (USA) Products LLC

Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...

The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Baxter Healthcare Corp.

Recalled Item: PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy...

The Issue: Presence of leaks near top of the PrismaSate bags

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2016· Ev3, Inc.

Recalled Item: EV3 EverFiex" Self-expanding Peripheral Stent System Recalled by Ev3, Inc....

The Issue: Medtronic is issuing a medical device recall to return product potentially...

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

Class II — Potential Health HazardOngoing
FoodMay 20, 2016· Ultimate Nutrition, Inc.

Recalled Item: ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· Ultimate Nutrition, Inc.

Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· Ultimate Nutrition, Inc.

Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· C.J. Dannemiller Company, Inc.

Recalled Item: The sunflower kernels roasted and salted were packed in a Recalled by C.J....

The Issue: Firm recalling under directions from their Supplier, due to possible risk of...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2016· C.J. Dannemiller Company, Inc.

Recalled Item: The sunflower kernels roasted ( no salt) were packed in Recalled by C.J....

The Issue: Firm recalling under directions from their Supplier, due to possible risk of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 20, 2016· Merz North America, Inc.

Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...

The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Amerx Health Care Corp.

Recalled Item: Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz....

The Issue: Product did not meet specifications for Zinc Acetate (OOS).

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2016· Integra LifeSciences Corp.

Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...

The Issue: The affected K-wires do not meet specification requirements. Specifically,...

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

Class II — Potential Health HazardOngoing