FDA Drug recall D-0241-2017
VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in C…
- FDA Drug
- Class III
- terminated
- Published 2017-01-04
On 2017-01-04 the FDA classified a Class III recall of VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in C… by Virtus Pharmaceuticals Opco Ii L, citing cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0241-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-12-12 |
| Published | 2017-01-04 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Virtus Pharmaceuticals Opco Ii L |
| Distribution | US |
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
cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.
Identifiers
| code_info | Lots #: 21506124 Exp. Date 5/30/2017, 21511151 Exp. date 10/30/2017, 21511151A Exp. Data 10/30/2017, 21512163 Exp. date…Lots #: 21506124 Exp. Date 5/30/2017, 21511151 Exp. date 10/30/2017, 21511151A Exp. Data 10/30/2017, 21512163 Exp. date 11/30/2017, 21512164 Exp. date 11/30/2017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0241-2017%22
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