BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Reported: May 3, 2017 Initiated: March 23, 2017 #F-2147-2017
Product Description
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.
Details
- Recalling Firm
- Armada Nutrition
- Units Affected
- 39,600 kg
- Distribution
- CO, NJ, England, South Africa,
- Location
- Spring Hill, TN
Frequently Asked Questions
What product was recalled? ▼
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe. Recalled by Armada Nutrition. Units affected: 39,600 kg.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 3, 2017. Severity: Moderate. Recall number: F-2147-2017.
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