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 3558135600 of 53,829 recalls

DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Cream Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2016· BAKE N JOY FOODS, INC.

Recalled Item: Bake'n Joy Sanding Sugar Net Wt. 16 lbs. pail Product Number: 0209416...

The Issue: Sanding sugar may contain metal fragments (supplier Domino Sugar)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2016· J&D's Down Home Enterprises, Inc.

Recalled Item: Original Bacon Flavored Seasoning Salt Recalled by J&D's Down Home...

The Issue: Original Bacon Flavored Seasoning Salt, Big Pig brand, is recalled due to a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Cepheid

Recalled Item: Xpert MRSA Catalog GXMRSA-120 Recalled by Cepheid Due to Internal...

The Issue: Internal investigation found the certain lots of MRSA kits have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...

The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, 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 DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, 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 DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Cranial S7. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, 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 DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...

The Issue: Medtronic Navigation, 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 DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, 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 DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...

The Issue: Medtronic Navigation, 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 DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
FoodJuly 16, 2016· ConAgra Frozen Foods, Inc

Recalled Item: PF Chang's Home Menu Brand Shrimp Lo Mein Recalled by ConAgra Frozen Foods,...

The Issue: Metal fragments were discovered in an raw ingredient used in the manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 15, 2016· The Harvard Drug Group

Recalled Item: Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative Recalled...

The Issue: Microbial contamination of Non-Sterile Products; positive findings of...

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

Class I — Serious Health HazardOngoing
Refund