Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Viva ben Femenine Supplement Recalled by Duy Drugs Inc. Due to Failure to meet with 21 CFR Part 111,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Duy Drugs Inc. directly.
Affected Products
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Quantity: 1800 bottles
Why Was This Recalled?
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Where Was This Sold?
Domestic distribution only.
About Duy Drugs Inc.
Duy Drugs Inc. has 2 total recalls tracked by RecallDetector.
Related Recalls
FSIS Issues Public Health Alert for Beef and Pork Products Produced Without the Benefit of Inspection
· March 27, 2026
FSIS Issues Public Health Alert for Ground Beef Products Due to Possible Foreign Material Contamination
· March 27, 2026
FSIS Issues Public Health Alert For Frozen Ready-To-Eat Turkey Stuffed Pastry Products Due To Misbranding
· March 27, 2026
Pork Dynasty Inc. Recalls Ready-to-Eat Fried Pork Skin Products Due to Misbranding and Undeclared Allergen
Pork Dynasty Inc. · March 27, 2026
Dearborn Sausage Company, Inc. Recalls Wiener Products Due to Misbranding and Undeclared Allergens
Dearborn Sausage Company, Inc. · March 27, 2026
Data sourced from the FDA (Food). Last updated March 26, 2026. View original report