Recalls / Class II
Class IIF-0296-2017
Product
GnuPharma Fit 100% Herbal Supplement 60 Capsules
- Type
- Food
- Affected lot / code info
- products manufactured prior to May 8th, 2017.
- Quantity
- 56 bottles
Why it was recalled
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Recalling firm
- Firm
- GnuPharma Corp.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 8751 N 117th East Ave Ste J, N/A, Owasso, Oklahoma 74055-2098
Distribution
- Distribution pattern
- US
Timeline
- Recall initiated
- 2017-05-08
- FDA classified
- 2017-07-18
- Posted by FDA
- 2017-07-26
- Terminated
- 2018-11-15
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0296-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.