FDAFDA · Food and drugs·Recall number F-0300-2017
GnuPharma Foundation 100% Herbal Supplement 60 Capsules
Published July 26, 2017 · Recall initiated: May 8, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- GnuPharma Corp.
- Distributor
- US
- Lot
- products manufactured prior to May 8th, 2017.
- Risk classification
- Class II
- Area (FDA)
- food
- Country
- United States
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