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GnuPharma Corp. recalls GnuPharma Relief 100% Herbal Supplement 60 Capsules
Recalled July 26, 2017 · FDA recall F-0297-2017 · GnuPharma
Hazard
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) · FDA Class II
Units
244 bottles
Sold at
US
Description
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Product
GnuPharma Relief 100% Herbal Supplement 60 Capsules
Manufacturer(s)
GnuPharma Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →