PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, UNFLAVOURED, (a) 30 SERVINGS
Recalling firm: Armada Nutrition
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 14, 2018.
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811274022038FDA code information
(a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM445515
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Full FDA record and distribution details
Original product description
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
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 811274022038 | INGS, Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02203 8 |
Original FDA recall 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.
Recall details
- Recall number
- F-2148-2017
- Event ID
- 76825
- FDA status
- Terminated
- Initiated
- Mar 23, 2017
- Reported
- May 3, 2017
- Classified
- Apr 27, 2017
- Terminated
- Feb 14, 2018
- Quantity
- 39,273 units
- Location
- Spring Hill, TN, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
CO, NJ, England, South Africa,
Data updated September 16, 2026. View official FDA data ↗
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