Cardiovid Plus 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 Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
- Recall number
- F-3356-2017
- 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
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
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