FDA Food recall F-2147-2017
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
- FDA Food
- Class II
- terminated
- Published 2017-05-03
On 2017-05-03 the FDA classified a Class II recall of BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe by Armada Nutrition, citing 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 lea….
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-2147-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-23 |
| Published | 2017-05-03 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Armada Nutrition |
| Distribution | CO, NJ |
Product
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Reason
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.
Identifiers
| code_info | lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2147-2017%22
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