Recalls / Class II
Class IIF-2147-2017
Product
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
- Type
- Food
- Affected lot / code info
- lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018
- Quantity
- 39,600 kg
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.
Recalling firm
- Firm
- Armada Nutrition
- Notification channel
- Telephone
- Type
- Voluntary: Firm initiated
- Address
- 4637 Port Royal Rd, N/A, Spring Hill, Tennessee 37174-2834
Distribution
- Distribution pattern
- CO, NJ, England, South Africa,
Timeline
- Recall initiated
- 2017-03-23
- FDA classified
- 2017-04-27
- Posted by FDA
- 2017-05-03
- Terminated
- 2018-02-14
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-2147-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.