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. 999 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
999 in last 12 months

Showing 37681–37700 of 53,829 recalls

FoodFebruary 11, 2016· Savory Foods, Inc.

Recalled Item: CARAMEL CORN PEANUT BUTTER DELIGHT¿ CRYSTAL SHORT (18 oz..) & Tall (22 oz..)...

The Issue: Savory Foods Inc. has initiated a voluntary recall due to the potential for...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: Valued Natural Raw Pistachio Kernels Net Wt 5 oz. (141 Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: IFS Web Bulk Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· Health Matters America, Inc.

Recalled Item: Organic traditions SPROUTED CHIA & FLAX SEED POWDER Recalled by Health...

The Issue: The repacked product has the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· Savory Foods, Inc.

Recalled Item: PRE-PORTION MASTER DOUGH (PEANUT BUTTER)- Raw cookie dough with 192...

The Issue: Savory Foods Inc. has initiated a voluntary recall due to the potential for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc.,...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing