Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 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.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 24, 2019.
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ProductCardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
FDA code information
Lot No. 1701
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Full FDA record and distribution details
Original product description
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Original FDA recall reason
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Recall details
- Recall number
- F-3356-2017
- Event ID
- 77715
- FDA status
- Terminated
- Initiated
- Jul 21, 2017
- Reported
- Aug 16, 2017
- Classified
- Aug 8, 2017
- Terminated
- Apr 24, 2019
- Quantity
- 411 bottles
- Location
- Doral, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
Domestic distribution only.
FDA source record · F-3356-2017
Data updated September 16, 2026. View official FDA data ↗
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