Myprotein Mypre V2
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…
Bulk Product Myprotein recall
Recalled by Armada Nutrition · Spring Hill, TN, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
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.
Pathogen: Staphylococcus
Staph bacteria that can produce heat-stable toxins.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Quantity: 39,600 kg
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018
Where it was sold
Colorado New Jersey
FDA's distribution note: CO, NJ, England, South Africa,
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Armada Nutrition
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 23, 2017
- In FDA report of
- May 3, 2017
- Terminated
- Feb 14, 2018
- FDA recall number
- F-2147-2017 · event 76825
- Official record
- FDA enforcement report search
Also recalled with it (6 more products)
FDA files each product of one recall action separately; these share the same FDA event.
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