GnuPharma Foundation 100% Herbal Supplement 60 Capsules
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0300-2017.
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0300-2017.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Gnupharma Corp. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0300-2017.
GnuPharma Corp.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Gnupharma Corp. Recall FAQ
Gnupharma Corp. is the subject of a supplements safety report: GnuPharma Foundation 100% Herbal Supplement 60 Capsules. The notice was published on May 8, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 9 units are potentially affected.