Viva ben Femenine Supplement recalled over manufacturing violations
- Recall date
- July 21, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Duy Drugs Inc. recalls Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
- Recall number
- F-3355-2017
- FDA classification
- Class II
- Brand / firm
- Duy Drugs Inc.
- Sold / distributed
- Domestic distribution only.
Why it was recalled
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
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