# FDA recall F-2148-2017

> **Armada Nutrition** · Class II · food recall initiated 2017-03-23.

## 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 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.

## Distribution

CO, NJ, England, South Africa,

## Key facts

- **Recall number:** F-2148-2017
- **Recalling firm:** Armada Nutrition
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2017-03-23
- **Report date:** 2017-05-03
- **Termination date:** 2018-02-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Spring Hill, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-2148-2017

## Citation

> AI Analytics. FDA recall F-2148-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/F-2148-2017. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
