FDA recall F-0297-2017
GnuPharma Corp. · Class II · food
Product
GnuPharma Relief 100% Herbal Supplement 60 Capsules
Reason for recall
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Distribution
US
Key facts
- Status
- Terminated
- Initiation date
- 2017-05-08
- Report date
- 2017-07-26
- Termination date
- 2018-11-15
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Owasso, OK, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0297-2017