Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Recalling firm: Duy Drugs Inc.
Why it was recalled
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
The exact product
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
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Original FDA code information
Lot No. 0117221
Recall details
- Recall number
- F-3355-2017
- Event ID
- 77715
- FDA status
- Terminated
- Initiated
- Jul 21, 2017
- Reported
- Aug 16, 2017
- Classified
- Aug 8, 2017
- Terminated
- Apr 24, 2019
- Quantity
- 1800 bottles
- Location
- Doral, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
Domestic distribution only.
FDA source record · F-3355-2017
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.