Armada Nutrition
Recall F-2147-2017 · Spring Hill, TN
Product
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Reason for recall
A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation was not properly conducted leaving concern that the finished product could contain the bacterium.
Distribution
CO, NJ, England, South Africa,
Quantity affected
39,600 kg
Recall type
Voluntary: Firm initiated
Lot / code info
lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018
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.
