# FDA recall D-0241-2017

> **VIRTUS PHARMACEUTICALS OPCO II L** · Class III · drug recall initiated 2016-12-12.

## Product

VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-348-30

## Reason for recall

cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0241-2017
- **Recalling firm:** VIRTUS PHARMACEUTICALS OPCO II L
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-12-12
- **Report date:** 2017-01-04
- **Termination date:** 2018-08-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Nashville, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0241-2017

## Citation

> AI Analytics. FDA recall D-0241-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0241-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
