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. 1,003 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,003 in last 12 months

Showing 36041–36060 of 53,829 recalls

FoodJune 2, 2016· The Quaker Oats Company

Recalled Item: Quaker Quinoa Granola Bars Recalled by The Quaker Oats Company Due to...

The Issue: SunOpta expanded their recall of listeria Monocytogenes in sunflower...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· Atlantic Spice Co., Inc.

Recalled Item: Atlantic Spice Tropical Mix Recalled by Atlantic Spice Co., Inc. Due to...

The Issue: Product was processed on the same equipment as product possibly contaminated...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· Ach Food Companies Inc

Recalled Item: Salad topping labeled under the following brand names: (Product 1) Recalled...

The Issue: Product manufactured with ingredient which may be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 2, 2016· Exact-Rx Inc

Recalled Item: Urea (50% Urea in a Cream Base) Recalled by Exact-Rx Inc Due to...

The Issue: Crystallization; complaints received by the manufacturer of crystals forming...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 1, 2016· Aidarex Pharmaceuticals LLC

Recalled Item: Ciprofloxacin OPTH 0.3% SOL Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 1, 2016· Becton Dickinson & Co.

Recalled Item: PhoenixSpec AP Calibrator is used to calibrate the PhoenixSpec &#38 Recalled...

The Issue: BD has determined that the PhoenixSpec AP Calibrator in this recall from the...

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

Class III — Low RiskOngoing
Medical DeviceJune 1, 2016· Becton Dickinson & Co.

Recalled Item: PhoenixSpec Calibrator & Kit is used to calibrate the PhoenixSpec Recalled...

The Issue: BD has determined that the BBL PhoenixSpec Calibrator kits in this recall...

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

Class III — Low RiskOngoing
Medical DeviceJune 1, 2016· Stryker Sustainability Solutions

Recalled Item: AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number:...

The Issue: Product defect; tip of two (2) Angiographic Catheters model # 10732203...

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

Class I — Serious Health HazardOngoing
FoodJune 1, 2016· Brown & Haley Inc.

Recalled Item: Mountain Thins Trail Mix flavor Recalled by Brown & Haley Inc. Due to...

The Issue: One additional lot of Mountain Thins Trail Mix flavor, net wt. 5.3 oz., is...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2016· Kellogg Company

Recalled Item: Kashi Whole Grain Bars 35 g individual bar Recalled by Kellogg Company Due...

The Issue: Product contains sunflower seeds potentially contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2016· Kellogg Company

Recalled Item: Bear Naked Soft Baked Granola Recalled by Kellogg Company Due to Potential...

The Issue: Product contains sunflower seeds potentially contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2016· Honey Bunchie, LLC

Recalled Item: Honey Bunchies Gourmet Honey Bars Recalled by Honey Bunchie, LLC Due to...

The Issue: Honey Bunchie, LLC is initiating a voluntary recall of a limited number of...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2016· Kellogg Company

Recalled Item: Kashi Whole Grain Trail Mix Bars 35 g individual bar Recalled by Kellogg...

The Issue: Product contains sunflower seeds potentially contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2016· Kellogg Company

Recalled Item: Kashi Chewy Trail Mix Granola Bars 1.2 oz individual bar Recalled by Kellogg...

The Issue: Product contains sunflower seeds potentially contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2016· Kellogg Company

Recalled Item: Bear Naked Soft Baked Granola Recalled by Kellogg Company Due to Potential...

The Issue: Product contains sunflower seeds potentially contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2016· Kellogg Company

Recalled Item: Kashi GOLEAN Honey Pecan Baklava Bars 1.59 oz. individual bar Recalled by...

The Issue: Product contains sunflower seeds potentially contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 31, 2016· Teva North America

Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva North America Due...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 31, 2016· Draeger Medical, Inc.

Recalled Item: Oxylog 3000 Recalled by Draeger Medical, Inc. Due to Isolated episodes of...

The Issue: Isolated episodes of leakage at the check valve were found

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.221 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.231 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing