GnuPharma Foundation 100% Herbal Supplement 60 Capsules — Class II food recall F-0300-2017
Terminated recall by GnuPharma Corp., reported 2017-07-26. 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
| Recall number | F-0300-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GnuPharma Corp., Owasso, OK, United States |
| Recall initiated | 2017-05-08 |
| Classified | 2017-07-18 |
| Reported by FDA | 2017-07-26 |
| Terminated | 2018-11-15 |
| Quantity | 9 bottles |
| Reason classes | microbial contamination |
| Pathogens | e coli |
Product
GnuPharma Foundation 100% Herbal Supplement 60 Capsules
Reason for recall
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-0300-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.