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. 1,090 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,090 in last 12 months

Showing 14981–15000 of 53,829 recalls

DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenol Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Mitomycin-C Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: LET Topical Gel Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Cantharidin PLUS Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: CSF-HC Otic Insufflation Capsule Recalled by Edge Pharma, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Methacholine Challenge 5-Syringe Test Kit Recalled by Edge Pharma, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Betadine (povidone-iodine) Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Gilead Sciences, Inc.

Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: investigation into a customer complaint...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles...

The Issue: Labeling: Missing Label

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Akorn, Inc. Due to...

The Issue: Labeling: Missing Label

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree sample boxes Recalled by Dental Alliance Holdings LLC Due to...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx7 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx21 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
FoodDecember 3, 2021· Slayer Forever, LLC dba BUBS Naturals

Recalled Item: BUBS Naturals Fountain of Youth Formula Recalled by Slayer Forever, LLC dba...

The Issue: Supplement contains undeclared milk from MCT oil powder ingredient.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 3, 2021· Konica Minolta Healthcare Americas, Inc.

Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...

The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2021· Wright Medical Technology Inc

Recalled Item: Stryker CLAW II ORTHOLOC 3DSi Plate Recalled by Wright Medical Technology...

The Issue: The incorrect product is contained in the packaging.

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

Class II — Potential Health HazardOngoing