Recalls / Class II
Class IIF-2148-2017
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
- Type
- Food
- Affected lot / code info
- (a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM445515
- Quantity
- 39,273 units
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.
Recalling firm
- Firm
- Armada Nutrition
- Notification channel
- Telephone
- Type
- Voluntary: Firm initiated
- Address
- 4637 Port Royal Rd, N/A, Spring Hill, Tennessee 37174-2834
Distribution
- Distribution pattern
- CO, NJ, England, South Africa,
Timeline
- Recall initiated
- 2017-03-23
- FDA classified
- 2017-04-27
- Posted by FDA
- 2017-05-03
- Terminated
- 2018-02-14
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-2148-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.