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RECALLING FIRM / COMPANY

Duy Drugs Inc. Recalls

Are there any recent recalls involving Duy Drugs Inc.?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

2 FDA product recordsLatest initiation: Jul 21, 2017

Same product name.
Different batch.
Check the label.

All recall records involving Duy Drugs Inc.

Initiated in 2017. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

2 recall recordsPage 1 of 1
Class II
FDA status: Terminated

Viva ben Femenine Supplement, Dietary Supplement 30 Softgels

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

OtherView details →
Class II
FDA status: Terminated

Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels

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

OtherView details →

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Same product name. Different batch. Details matter.

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