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