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Class II: temporary or reversible health riskTerminated

Armada Nutrition Bulk Product: Myprotein Recall

BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in…

Armada Nutrition · Spring Hill, TN

Risk level
Class II
Reported by FDA
May 3, 2017
Recall ID
F-2147-2017
Check your lot numberHow we source this data

Summary

Armada Nutrition recalled Bulk Product: Myprotein starting Mar 23, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2147-2017 on May 3, 2017. 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 could contain the bacterium. Status: Terminated.

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.

Product description

BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe

Lot numbers, UPCs & expiration codes

lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018

Where it was sold

CO, NJ, England, South Africa,

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2147-2017
Classification
Class II
Status
Terminated
Recall initiated
Mar 23, 2017
FDA report date
May 3, 2017
Quantity
39,600 kg
Recall type
Voluntary: Firm initiated
Recalling firm
Armada Nutrition

Original FDA data

Every field from FDA enforcement report F-2147-2017, exactly as published.

Show all FDA fields
City
Spring Hill
State
TN
Status
Terminated
Country
United States
Event ID
76825
Address
4637 Port Royal Rd
Code information
lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/2018
Postal code
37174-2834
Report date
May 3, 2017
Product type
Food
Recall number
F-2147-2017
Classification
Class II
Recalling firm
Armada Nutrition
Product quantity
39,600 kg
Termination date
Feb 14, 2018
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe
Distribution pattern
CO, NJ, England, South Africa,
Recall initiation date
Mar 23, 2017
Initial firm notification
Telephone
Center classification date
Apr 27, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2147-2017, published May 3, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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