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Armada Nutrition
FDA recall F-2148-2017 · Class II · reported 2017-05-03 · Terminated
- Product
- PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, UNFLAVOURED, (a) 30 SERVINGS, UPC 8 11274 02239 8; (b) 45 SERVINGS, Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02203 8
- 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.
- Quantity
- 39,273 units
- Distribution
- CO, NJ, England, South Africa,
- Firm location
- TN, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Telephone
- Recall started
- 2017-03-23
- Terminated
- 2018-02-14
- Code info
- (a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM445515
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.