Virt-Nate Prenatal/Postnatal — Class III drug recall D-0775-2016
Terminated recall by Virtus Pharmaceuticals, Llc, reported 2016-03-23, distributed in MI. Tablets/Capsules Imprinted with Wrong ID; product debossed with an incorrect punch. Bottles could contain tabl
| Recall number | D-0775-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Virtus Pharmaceuticals, Llc, Tampa, FL, United States |
| Recall initiated | 2016-01-15 |
| Classified | 2016-03-14 |
| Reported by FDA | 2016-03-23 |
| Terminated | 2018-08-21 |
| Distributed | MI |
| Quantity | 1,139 bottles |
| UPC / GTIN / UDI-DI | 00376439264109 |
| NDC | 69543-0264-10, 76439-0264-10 |
| Lot numbers | M143810, M143810A |
| Expiration dates | 2017-07 |
Product
Virt-Nate Prenatal/Postnatal, Prescription Folate-Containing Dietary Supplement, Rx, 100 count bottles, Manufactured For: Virtus Pharmaceuticals, Tampa, FL
Reason for recall
Tablets/Capsules Imprinted with Wrong ID; product debossed with an incorrect punch. Bottles could contain tablets debossed with V259 (debossing for PreTab) instead of the correct punch, V264 (debossing for Virt-Nate).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0775-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.