Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Virt-Advance Prenatal/Postnatal Softgels Recalled by VIRTUS PHARMACEUTICALS OPCO II L Due to cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is...

Date: December 12, 2016
Company: VIRTUS PHARMACEUTICALS OPCO II L
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact VIRTUS PHARMACEUTICALS OPCO II L directly.

Affected Products

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

Quantity: 2,537 bottles

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About VIRTUS PHARMACEUTICALS OPCO II L

VIRTUS PHARMACEUTICALS OPCO II L has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report