Severity
Low
FDA Food recall · Reported September 12, 2018
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 cor…
Virtus Pharmaceuticals LLC. recalled Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bo… - a low-severity action.
Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bo… was recalled by Virtus Pharmaceuticals LLC. in September 12, 2018. Reason: Virtus Pharmaceuticals, LLC has decided to initiate a recall of the following products : Virt-Nate Tablets …. Check the official notice for the remedy. Verify recall #F-1932-2018 with the FDA Food before acting.
The recall
Virtus Pharmaceuticals LLC. issued this low-severity FDA Food recall-Virtus Pharmaceuticals, LLC has decided to initiate a recall of the following products : Virt-Nate Tablets ….
Sourced from official FDA Food enforcement records. Verify recall #F-1932-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1932-2018) was formally reported on September 12, 2018, with the manufacturer initiating the action on August 3, 2018. It is classified under Low severity (Class III), with a current status of Terminated. Virtus Pharmaceuticals LLC. is listed as the recalling firm, operating out of Newtown, PA. Federal records list the affected scope as 2209 Bottles.
The documented reason for this recall is: 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 Equivalent… Distribution data in the federal record shows the product reached: 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, Cali…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
2209 Bottles
Related Recalls
6
0 from same agency
Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle
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.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-1932-2018 |
| Date reported | September 12, 2018 |
| Date initiated | August 3, 2018 |
| Recalling firm | Virtus Pharmaceuticals LLC. |
| Firm location | Newtown, PA |
| Affected scope | 2209 Bottles |
| Distribution | 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, Fl… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 12, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.