# FDA recall F-3356-2017

> **Duy Drugs Inc.** · Class II · food recall initiated 2017-07-21.

## 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.

## Distribution

Domestic distribution only.

## Key facts

- **Recall number:** F-3356-2017
- **Recalling firm:** Duy Drugs Inc.
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2017-07-21
- **Report date:** 2017-08-16
- **Termination date:** 2019-04-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Doral, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-3356-2017

## Citation

> AI Analytics. FDA recall F-3356-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/F-3356-2017. Source: US FDA. Licensed CC0.

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