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. 1,020 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,020 in last 12 months

Showing 28721–28740 of 53,829 recalls

DrugFebruary 28, 2018· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 28, 2018· Blue Moose of Boulder, LLC

Recalled Item: All-Natural Ciolo Nut-Free Basil Pesto Recalled by Blue Moose of Boulder,...

The Issue: Firm is recalling Nut-Free Basil Pesto due to mislabeling, causing...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Green Tea Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Lemongrass Facial Polish with Oats Recalled by Plant Devas Inc Due to FDA...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Rose Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of Colors...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Clay Mask Kit Recalled by Plant Devas Inc Due to FDA Office of Colors and...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Blue Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of Colors...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Blemish Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Ayurvedic Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: French Rose Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD has...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Integrity Implants Inc.

Recalled Item: FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System)...

The Issue: Recently Integrity Implants uncovered a discrepancy in the cleaning...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Adult/Pediatric Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Helena Laboratories, Corp.

Recalled Item: SPIFE Alkaline Hemoglobin Kit Recalled by Helena Laboratories, Corp. Due to...

The Issue: Lots of gel kits contained a newer revision of the Customer Procedures...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Radiometer Medical ApS

Recalled Item: AQURE Recalled by Radiometer Medical ApS Due to There is a potential problem...

The Issue: There is a potential problem relating to the AQURE System, versions 2.3.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2018· Genesee BioMedical, Inc.

Recalled Item: Sternal Valve Retractors With Atrial and Aortic Rakes Recalled by Genesee...

The Issue: Failure in a retractor blade due to corrosion. In the area of the blade...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2018· Beaver-Visitec International Inc.

Recalled Item: Wet-Field Hemostatic Eraser Bipolar 25G Recalled by Beaver-Visitec...

The Issue: Products were packaged with incorrect labeling,

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2018· Mckesson Packaging Services

Recalled Item: RANITIDINE Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund