Viva ben Femenine Supplement recall: CGMP Deviations
Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
Why was Viva ben Femenine Supplement recalled?
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot No. 0117221
- Product
- Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
- Recalling firm
- Duy Drugs Inc.
- Quantity
- 1800 bottles
- Distribution
- Domestic distribution only.
- Recall date
- August 16, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (food)