Duy Drugs Recalls Viva ben Femenine Supplement for CGMP Violations
Duy Drugs Inc. is recalling 1,800 bottles of Viva ben Femenine Supplement because the product failed to meet current good manufacturing practices (CGMPs) for identity, purity, and composition.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II due to CGMP violations regarding identity, purity, and composition. Per the rubric, this falls under 'Moderate' as it involves a voluntary precautionary recall for manufacturing standards without reported illnesses or specific high-risk pathogens.
Plain-English summary
Duy Drugs Inc. is voluntarily recalling 1,800 bottles of Viva ben Femenine Supplement, a dietary supplement containing 30 softgels. The recall was initiated because the product failed to meet the requirements of 21 CFR Part 111, which outlines current good manufacturing practices (CGMPs) for dietary supplements. Specifically, the failure involved assuring the identity, purity, and composition of the product.
The affected product is identified by Lot No. 0117221. The recall covers domestic distribution only. The U.S. Food and Drug Administration has classified this recall as Class II, indicating that use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Consumers who have purchased this product should stop using it and return it to the place of purchase for a refund or contact the recalling firm for further instructions. No specific illnesses or injuries have been reported in the source text.
The recalled product
- Product
- Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
- Manufacturer
- Duy Drugs Inc.
- Category
- Food — Dietary Supplement
- Affected units
- 1,800
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot No. 0117221
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 2 recalled by Duy Drugs Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Duy Drugs Inc.
See all →- ModerateDuy Drugs Recalls Cardiovid Plus Dietary Supplement for CGMP Violations
FDA (Food) · 2017-08-16
Same hazard · cgmp violation
See all →- Moderatevite20 Antifungal Cream recalled due to stability testing deviations
FDA (Drugs) · 2026-07-08
- ModerateNeuroquell products recalled over current good manufacturing practice violations
FDA (Drugs) · 2025-09-17
- ModerateOptim V Anti-Itch Cream Recalled for Current Good Manufacturing Practice Deviations
FDA (Drugs) · 2025-05-28
- ModerateNature Mint Anticavity Fluoride Toothpaste Recalled for CGMP Deviations
FDA (Drugs) · 2025-05-28
- ModerateRapidol Hydrocortisone 1% Anti-Itch Cream Recalled for CGMP Deviations
FDA (Drugs) · 2025-05-28