Recall · openFDA Food Enforcement

Viva ben Femenine Supplement, Dietary Supplement 30 Softgels: FDA Recall F-3355-2017

Agency action: Jul 21, 2017Record ID: F-3355-2017
View official source ↗

What happened

Original notice title

Viva ben Femenine Supplement, Dietary Supplement 30 Softgels, recall F-3355-2017

From the archived source record

Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Aug 16, 2017
Termination date in the archive
Apr 24, 2019
Source checked
Jul 16, 2026
Record revision
eb709373afdf

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Company
Duy Drugs Inc.
Lot / identifier
Lot No. 0117221
Market / distribution
Domestic distribution only.