PERFORMIX — Class II food recall F-2152-2017
Terminated recall by Armada Nutrition, reported 2017-05-03, distributed in CO, NJ. A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but
| Recall number | F-2152-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Armada Nutrition, Spring Hill, TN, United States |
| Recall initiated | 2017-03-23 |
| Classified | 2017-04-27 |
| Reported by FDA | 2017-05-03 |
| Terminated | 2018-02-14 |
| Distributed | CO, NJ |
| Countries outside the US | GB, ZA |
| Quantity | 19,552 units |
| Reason classes | specification failure |
| Pathogens | staphylococcus |
| UPC / GTIN / UDI-DI | 00811274022045 |
| Lot numbers | IM442915 |
| Expiration dates | 2018-08 |
Product
PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, BLUE RAZZ ICE, NET WT 11.1 OZ (315G), Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02204 5
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-2152-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.