Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 21, 2017 (9 years ago)

Cardiovid Plus Cardiovascular Active Dietary Supplement recall

Recalled by Duy Drugs Inc. · Doral, FL, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels

Quantity: 411 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot No. 1701

Where it was sold

FDA's distribution note: Domestic distribution only.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Duy Drugs Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 21, 2017
In FDA report of
Aug 16, 2017
Terminated
Apr 24, 2019
FDA recall number
F-3356-2017 · event 77715
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Processing

Viva ben Femenine Supplement

Reason Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.

Duy Drugs Inc. F-3355-2017

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