Home / Duy Drugs Inc. / F-3355-2017
Class II
Duy Drugs Inc.
Recall #F-3355-2017 · Initiated 2017-07-21
Product
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.
Quantity affected
1800 bottles
Distribution
Domestic distribution only.
Lot / code info
Lot No. 0117221
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
E-Mail
Terminated
2019-04-24
Recalling firm
Duy Drugs Inc.
1730 NW 79th Ave
Doral, FL 33126-1111
United States
Recall classification
Remote probability of serious adverse health consequences, or temporary reversible consequences.