CLASS II Food recall · Reported 3 May 2017 · FDA Enforcement Report

Performix(TM) Crea-bead, Multi-phase Creatine, Unflavoured, (a) recalled

Armada Nutrition is recalling Performix(TM) Crea-bead, Multi-phase Creatine, Unflavoured, (a), distributed in Colorado, New Jersey. The recall was initiated on 23 Mar 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes(a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM445515
Quantity recalled39,273 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2148-2017
FDA event ID
76825
Recalling firm
Armada Nutrition, Spring Hill, TN
Classification
Class II
Status
Terminated
Recall initiated
23 Mar 2017
FDA classified
27 Apr 2017
Reported
3 May 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Product category
Other

Timeline

23 Mar 2017Recall initiated by company
27 Apr 2017Classified by FDA+35 days
3 May 2017Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Product as listed by the FDA

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

Where it was distributed

CO, NJ, England, South Africa,

ColoradoNew Jersey

Questions about this recall

Why was it 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.

Which lots are affected?

(a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM445515

Where was it sold?

CO, NJ, England, South Africa,

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 76825

This product is part of a recall event; the main page for the event is Mp Musclepharm, Assault, Energy + Strength recalled by Armada Nutrition.

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