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…
Usn B4 -Bomb Extreme Pre-Workout 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
USN B4 -BOMB EXTREME PRE-WORKOUT, LIME LEMONADE FLAVOUR, 300g, USN North America, 1560 Sawgrass Corporation Pkwy, 4th Floor, Sunrise, FL, 33323
Quantity: 3,997 units
Food: Juice & beverages
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 IM453078, Exp 08/2018
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-2149-2017 · 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.
Bulk Product Myprotein
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…
Performix (tm) Crea-Bead
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…
Muscle Meds (TM) PERFORMANCE TECHNOLOGIES
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…
Mp Musclepharm Assault
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…
Performix (tm) Crea-Bead
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…
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