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 1162111640 of 13,439 recalls

DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Ex DROPS 5X Recalled by Terra-Medica Inc. 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
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. 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
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Quent DROPS 5X Recalled by Terra-Medica Inc. 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
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. 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
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Quent CAPSULES 4X Recalled by Terra-Medica Inc. 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
DrugFebruary 26, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...

The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge and NicoDerm CQ Recalled by GlaxoSmithKline Consumer...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2014· Gilead Sciences, Inc.

Recalled Item: Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil...

The Issue: Presence of Foreign Substance: Red Silicone Rubber Particulates are Present...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 14, 2014· Agila Specialties Private Ltd.

Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...

The Issue: Presence of Particulate Matter: Potential for small black particles to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2014· Legacy Pharmaceutical Packaging

Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...

The Issue: Chemical Contamination: The recalling firm received notice that their...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2014· Ben Venue Laboratories Inc

Recalled Item: Acetylcysteine Solution Recalled by Ben Venue Laboratories Inc Due to...

The Issue: Presence of Particulate Matter: During a review of retain samples, the firm...

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

Class I — Serious Health HazardOngoing
Refund