US Food Recall Atlas

A single recall record, as the agency published it.

Recall map → All recalls → F-1933-2018

Virt Gard Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle VIRTUS PHARMACEUTICALS LLC. · reported 2018-09-12

Terminated This recall has been closed out by the agency.

Reason for recall
Virtus Pharmaceuticals, LLC has decided to initiate a recall of the following products : Virt-Nate Tablets and Virt Gard Tablets because product labels do not reflect the correct amount of Dietary Folate Equivalents (DFEs) calculated based on the product formulation.
Classification
Class III
Recall initiated
2018-08-03
Reported by the agency
2018-09-12
Closed out (terminated)
2019-04-06
Recalling firm
VIRTUS PHARMACEUTICALS LLC.
Newtown, PA
United States

This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.

Distribution (the agency's own words)
Virt Nate: Arizona, Colorado, Illinois, Indiana, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Texas, Virginia, Vermont and Wisconsin. Virt Gard: Arizona, California, Colorado, Florida, Georgia, Iowa, Illinois, Kentucky, Massachusetts, Michigan, Missouri, Mississippi, North Carolina, New Jersey, New York, Ohio, Pennsylvania, South Carolina, Texas, Virginia and West Virginia.
States we parsed from that text
AZ CA CO FL GA IA IL IN KY MA MI MN MO MS NC NJ NY OH OK PA SC TX VA VT WI WV

The agency named these states. Parse method explicit_state_list, confidence high.

Food category
Dietary supplementsderived

Assigned by a reviewed keyword rulebook over the product description, not by the agency.

Recall type
Voluntary: Firm initiated
Recall number
F-1933-2018

View this record at the agency source →

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.