Drug recall
Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with…
FDA recall event 76103 · Class III · VIRTUS PHARMACEUTICALS OPCO II L
Key facts
| Event ID | 76103 |
|---|---|
| Recall numbers | D-0238-2017, D-0239-2017, D-0240-2017, D-0241-2017 |
| Recalling firm | VIRTUS PHARMACEUTICALS OPCO II L |
| Product type | Drugs |
| Products | Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-251-30, Virt-Advance Prenatal/Postnatal Softgels, Prescription Folic Acid Containing Dietary Supplement, packaged in 90-count bottle, Rx only, Made in Canada, NDC 76439-357-90, 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, Virt-Select Prenatal/Postnatal Softgels, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-249-30 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert. |
| Initiation date | Dec 12, 2016 |
| Report date | Jan 4, 2017 |
| Termination date | Aug 21, 2018 |
| City | Nashville |
| State | TN |
| Country | United States |
| FEI number | 3012444225 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: