CLASS II Food recall · Reported 16 Aug 2017 · FDA Enforcement Report
Viva ben Femenine Supplement, Dietary Supplement recalled by Duy Drugs
Duy Drugs is recalling Viva ben Femenine Supplement, Dietary Supplement. The recall was initiated on 21 Jul 2017 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-3355-2017
- FDA event ID
- 77715
- Recalling firm
- Duy Drugs, Doral, FL
- Brand
- Viva
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 21 Jul 2017
- FDA classified
- 8 Aug 2017
- Reported
- 16 Aug 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Manufacturing (CGMP) Deviations
- Product category
- Dietary Supplements
Timeline
| 21 Jul 2017 | Recall initiated by company | |
| 8 Aug 2017 | Classified by FDA | +18 days |
| 16 Aug 2017 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Product as listed by the FDA
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Where it was distributed
Domestic distribution only.
Questions about this recall
Why was it recalled?
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Which lots are affected?
Lot No. 0117221
Where was it sold?
Domestic distribution only.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 77715This product is part of a recall event; the main page for the event is Cardiovid Plus, Cardiovascular Active Dietary Supplement recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Cardiovid Plus, Cardiovascular Active Dietary Supplement recalledCardiovid Plus | Duy Drugs | Manufacturing (CGMP) Deviations | FL |
More recalls from Duy Drugs
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Cardiovid Plus, Cardiovascular Active Dietary Supplement recalledCardiovid Plus | Duy Drugs | Manufacturing (CGMP) Deviations | FL |
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