FDA recall record
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 24, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Reason
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Code information listed by FDA
Lot No. 1701
Distribution and firm information
Recalling firm listed by FDA: Duy Drugs Inc.
Firm location listed by FDA: Doral, FL, United States
Distribution reported by FDA: Domestic distribution only.
Product quantity listed by FDA: 411 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.