Terminated Class II

GnuPharma Corp.

Recall F-0296-2017 · Owasso, OK

Product

GnuPharma Fit 100% Herbal Supplement 60 Capsules

Reason for recall

1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

Distribution

US

Quantity affected

56 bottles

Recall type

Voluntary: Firm initiated

Lot / code info

products manufactured prior to May 8th, 2017.

Timeline

8 May 2017 initiated → 18 Jul 2017 classified → 26 Jul 2017 reported → 15 Nov 2018 terminated

Sourced directly from the FDA’s openFDA enforcement database. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.