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Duy Drugs Inc.
FDA recall F-3355-2017 · Class II · reported 2017-08-16 · Terminated
- Product
- Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
- Reason
- Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
- Quantity
- 1800 bottles
- Distribution
- Domestic distribution only.
- Firm location
- FL, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Recall started
- 2017-07-21
- Terminated
- 2019-04-24
- Code info
- Lot No. 0117221
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.