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GnuPharma Corp.
FDA recall F-0301-2017 · Class II · reported 2017-07-26 · Terminated
- Product
- GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
- Reason
- 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
- Quantity
- 1 unit (4 tablespoons)
- Distribution
- US
- Firm location
- OK, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Recall started
- 2017-05-08
- Terminated
- 2018-11-15
- Code info
- products manufactured prior to May 8th, 2017.
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.