US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 15, 2016 (11 years ago)

Virt-Nate Prenatal/Postnatal

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

Why it was recalled

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).

What was recalled

Virt-Nate Prenatal/Postnatal, Prescription Folate-Containing Dietary Supplement, Rx, 100 count bottles, Manufactured For: Virtus Pharmaceuticals, Tampa, FL

Recalling firm
Virtus Pharmaceuticals, Llc
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0775-2016

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.