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Armada Nutrition recalls BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Recalled May 3, 2017 · FDA recall F-2147-2017 · Armada Nutrition
Hazard
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. · FDA Class II
Units
39,600 kg
Sold at
CO, NJ, England, South Africa,
Description
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.
Product
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Manufacturer(s)
Armada Nutrition
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →