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. 2,803 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,803 in last 12 months

Showing 96419660 of 13,439 recalls

DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Black Widow 25 Ephedra Super Potent Fat Burner Dietary Supplement Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Fataway Ultimate Stack with Chromium Recalled by Novacare, LLC...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim MaxOut Body Max Out FX Fat Burner Recalled by Novacare, LLC...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Naturally The Natural Alternative AM Dietary Supplement...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Xcellerator (product not labeled) Recalled by Novacare, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: Lacri-Lube (Mineral Oil 42.5% and White Petrolatum 56.8%) Lubricant Recalled...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: MetaPro 360 Metabolic Accelerator Dietary Supplement packaged in 120 capsule...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Recalled by...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution...

The Issue: Lack of Assurance of Sterility; potential exposure to non-sterile lubricant...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: HEPARIN Sodium in 0.45% Sodium Chloride Recalled by Cantrell Drug Company...

The Issue: Stability Data Does Not Support Expiry

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection Recalled by...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection Recalled by Cantrell...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL Citrate 50 mcg/mL in Sterile Water for Injection Recalled by...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: MIDAZOLAM HCl in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Silarx Pharmaceutical, Inc.

Recalled Item: Lamivudine Oral Solution Recalled by Silarx Pharmaceutical, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a...

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

Class III — Low RiskOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: Midazolam HCl in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund