BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Recalling firm: Armada Nutrition
Why it was recalled
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.
The exact product
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Check the codes
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Original FDA code information
lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018
Recall details
- Recall number
- F-2147-2017
- Event ID
- 76825
- FDA status
- Terminated
- Initiated
- Mar 23, 2017
- Reported
- May 3, 2017
- Classified
- Apr 27, 2017
- Terminated
- Feb 14, 2018
- Quantity
- 39,600 kg
- Location
- Spring Hill, TN, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
CO, NJ, England, South Africa,
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.