Cardiovid Plus — Class II food recall F-3356-2017
Terminated recall by Duy Drugs Inc., reported 2017-08-16. Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements
| Recall number | F-3356-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Duy Drugs Inc., Doral, FL, United States |
| Recall initiated | 2017-07-21 |
| Classified | 2017-08-08 |
| Reported by FDA | 2017-08-16 |
| Terminated | 2019-04-24 |
| Quantity | 411 bottles |
| Lot numbers | 1701 |
Product
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Reason for recall
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-3356-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.