MODERATE RISK
Terminated
F-3355-2017
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Recalled by Duy Drugs Inc.
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
Reason for Recall
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Product Details
Product Quantity
1800 bottles
Product Type
Food
Code Info
Lot No. 0117221
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Domestic distribution only.
Company Location
Doral, FL, 33126-1111
Timeline
Report Date
08/16/2017
Recall Initiated
07/21/2017
Classification Date
08/08/2017
Termination Date
04/24/2019
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 29, 2026
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