Class IITerminated in FDA datasetRecall initiated Mar 23, 2017

Muscle Meds(TM) PERFORMANCE TECHNOLOGIES, BIOENGINEERED BEEF PROTEIN ISOLATE CARNIVOR(TM)…

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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 14, 2018.

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ProductMuscle Meds(TM) PERFORMANCE TECHNOLOGIES, BIOENGINEERED BEEF PROTEIN ISOLATE CARNIVOR(TM) Dietary Supplement, Net Wt. 2 lbs. (904.4g), ADVANCED FLAVOR TECHNOOGY FRUIT PUNCH, (a) 904.4g, (b)1808.8g, Manufactured for and Distributed by: MuscleMeds Performace Technologies 165 Clayton Road, West Caldwell, NJ 07006, UPC 08 91597 00214 6
Package size2 lbs

FDA code information

(a) lot IM445587, Exp 07/2019 (b) lot IM449808, Exp 07/2019

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Full FDA record and distribution details

Original product description

Muscle Meds(TM) PERFORMANCE TECHNOLOGIES, BIOENGINEERED BEEF PROTEIN ISOLATE CARNIVOR(TM) Dietary Supplement, Net Wt. 2 lbs. (904.4g), ADVANCED FLAVOR TECHNOOGY FRUIT PUNCH, (a) 904.4g, (b)1808.8g, Manufactured for and Distributed by: MuscleMeds Performace Technologies 165 Clayton Road, West Caldwell, NJ 07006, UPC 08 91597 00214 6

Original FDA recall reason

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.

Recall details

Recall number
F-2150-2017
Event ID
76825
FDA status
Terminated
Initiated
Mar 23, 2017
Reported
May 3, 2017
Classified
Apr 27, 2017
Terminated
Feb 14, 2018
Quantity
1884 units
Location
Spring Hill, TN, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

CO, NJ, England, South Africa,

FDA source record · F-2150-2017

Data updated September 16, 2026. View official FDA data ↗

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