US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 12, 2016 (10 years ago)

VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

What was recalled

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

Recalling firm
Virtus Pharmaceuticals Opco II L
NDC code
76439-348-30
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0241-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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