GnuPharma Corp.
Recall F-0301-2017 · Owasso, OK
Product
GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
Reason for recall
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Distribution
US
Quantity affected
1 unit (4 tablespoons)
Recall type
Voluntary: Firm initiated
Lot / code info
products manufactured prior to May 8th, 2017.
Timeline
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.
