Duy Drugs Recalls Cardiovid Plus Due to Quality Control Failures
Duy Drugs Inc. recalls Cardiovid Plus dietary supplements because they may not meet federal quality standards for identity, purity, and composition.
Use caution until it’s fixed
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Contact the company
What happened, in plain English
Duy Drugs Inc. is recalling Cardiovid Plus, a cardiovascular active dietary supplement sold in 60-softgel bottles. The recall addresses failures to comply with Current Good Manufacturing Practices (CGMPs), meaning the product may not have the correct identity, purity, or composition it claims. This means consumers cannot be sure what ingredients are actually inside the bottle. Read more at govinfonow.com/recall/20648-duy-drugs-recalls-cardiovid-plus-due-to-quality-control-failures.
Source Summary by GovInfoNow · govinfonow.com/recall/20648-duy-drugs-recalls-cardiovid-plus-due-to-quality-control-failures · Updated October 11, 2026 · FDA enforcement record: FDA #F-3356-2017
Cite this page
“Duy Drugs Recalls Cardiovid Plus Due to Quality Control Failures.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20648-duy-drugs-recalls-cardiovid-plus-due-to-quality-control-failures. Based on FDA recall #F-3356-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3356-2017%22&limit=1).
Why it’s dangerous
The product failed to meet federal regulations ensuring that dietary supplements contain exactly what is listed on the label in terms of identity, purity, and composition. This lack of quality control could result in the supplement containing incorrect ingredients or impurities.
Who’s affected
Consumers who purchased Cardiovid Plus dietary supplements, specifically those with Lot No. 1701, are affected by this recall.
How to tell if you have this one
Check your bottle for the brand name Cardiovid Plus, labeled as a Cardiovascular Active Dietary Supplement containing 60 softgels. Verify if the Lot Number is 1701. The product was distributed domestically within the United States.
- Brand
Duy Drugs- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Domestic distribution only.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-3355-2017 | Viva ben Femenine Supplement, Dietary Supplement 30 Softgels; Lot No. 0117221 | 1800 bottles |
| F-3356-2017 | Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels; Lot No. 1701 | 411 bottles |
How this recall unfolded
Recall timeline
FDA terminated this recall 21 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-3356-2017 (July 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3356-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.