Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported August 16, 2017
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.
Duy Drugs Inc. recalled Viva ben Femenine Supplement, Dietary Supplement 30 Softgels - a moderate-severity action.
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels was recalled by Duy Drugs Inc. in August 16, 2017. Reason: Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplement…. Check the official notice for the remedy. Verify recall #F-3355-2017 with the FDA Food before acting.
The recall
Duy Drugs Inc. issued this moderate-severity FDA Food recall-Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplement….
- Moderate
- severity level
- Class II
- classification
- August 16, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-3355-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-3355-2017) was formally reported on August 16, 2017, with the manufacturer initiating the action on July 21, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Duy Drugs Inc. is listed as the recalling firm, operating out of Doral, FL. Federal records list the affected scope as 1800 bottles.
The documented reason for this recall is: Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements. Distribution data in the federal record shows the product reached: Domestic distribution only.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1800 bottles
Related Recalls
6
6 from same agency
Product description
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Reason for recall
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-3355-2017 |
| Date reported | August 16, 2017 |
| Date initiated | July 21, 2017 |
| Recalling firm | Duy Drugs Inc. |
| Firm location | Doral, FL |
| Affected scope | 1800 bottles |
| Distribution | Domestic distribution only. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-3355-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels. Recalled by Duy Drugs Inc.. Units affected: 1800 bottles.
Why was this product recalled? ▼
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on August 16, 2017. Severity: Moderate. Recall number: F-3355-2017.
Where was the recalled product distributed? ▼
Distribution: Domestic distribution only..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-3355-2017) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported August 16, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.