FDA recall F-3355-2017
Duy Drugs Inc. · Class II · food
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.
Distribution
Domestic distribution only.
Key facts
- Status
- Terminated
- Initiation date
- 2017-07-21
- Report date
- 2017-08-16
- Termination date
- 2019-04-24
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Doral, FL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-3355-2017