PlainRecalls
FDA Food Moderate Class II Terminated

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.