PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, UNFLAVOURED, (a) 30 SERVINGS
Recalling firm: Armada Nutrition
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.
The exact 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
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Original FDA code information
(a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM445515
| Type | Code / value | Context |
|---|---|---|
| UPC | 811274022038 | INGS, Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02203 8 |
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 ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.