GnuPharma Relief 100% Herbal Supplement 60 Capsules recalled over E. coli risk
- Recall date
- May 8, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- GnuPharma Corp. recalls GnuPharma Relief 100% Herbal Supplement 60 Capsules
- Recall number
- F-0297-2017
- FDA classification
- Class II
- Brand / firm
- GnuPharma Corp.
- Sold / distributed
- US
Why it was recalled
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
GnuPharma Relief 100% Herbal Supplement 60 Capsules
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