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. 2,796 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,796 in last 12 months

Showing 1164111660 of 13,439 recalls

DrugFebruary 14, 2014· Medisca Inc

Recalled Item: CITRULLINE (L) in 25 g Recalled by Medisca Inc Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2014· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2014· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2014· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2014· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 11, 2014· Viiv Healthcare Company

Recalled Item: Tivicay (dolutegravir) Tablets 50 mg Recalled by Viiv Healthcare Company Due...

The Issue: Cross Contamination with Other Products: Product contains Promacta...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 11, 2014· Teva Pharmaceuticals USA

Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 11, 2014· Baxter Healthcare Corp.

Recalled Item: Dianeal PD-2 Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Non-Sterility: Complaints of leaks and particulate matter identified as mold...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 11, 2014· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility:Solution leaking through the port cover of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2014· Hospira Inc.

Recalled Item: Bupivacaine HCl Inj. USP Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer report of visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2014· Actavis Elizabeth LLC

Recalled Item: Alprazolam 1 mg Tablets Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Complaints were received for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2014· Pinnacle Biologics Inc

Recalled Item: Photofrin (porfimer sodium) for Injection Recalled by Pinnacle Biologics Inc...

The Issue: Stability Data Does Not Support Expiry: Printed expiration date should be...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 7, 2014· Actavis

Recalled Item: Gelnique (oxybutynin chloride) Gel 10% Recalled by Actavis Due to Subpotent...

The Issue: Subpotent Drug: Drug potency was compromised during shipment.

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

Class III — Low RiskOngoing
Refund
DrugFebruary 4, 2014· Aaron Industries Inc

Recalled Item: Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan...

The Issue: Presence of Precipitate: Recall is due to complaints of a white substance,...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 4, 2014· Actavis Elizabeth LLC

Recalled Item: Alprazolam Extended-Release Tablets Recalled by Actavis Elizabeth LLC Due to...

The Issue: Failed Dissolution Specifications: Product did not meet specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops Recalled by Hill...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· American Health Packaging

Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% (Scalp...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund