FDA recall record
GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of November 15, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
Reason
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
Code information listed by FDA
products manufactured prior to May 8th, 2017.
Distribution and firm information
Recalling firm listed by FDA: GnuPharma Corp.
Firm location listed by FDA: Owasso, OK, United States
Distribution reported by FDA: US
Product quantity listed by FDA: 1 unit (4 tablespoons)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.