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Recall Radar/FDA Food Enforcement/F-2150-2017

FDA Food EnforcementMedium / 中

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

Recall F-2150-2017Published 2017-05-03Company Armada Nutrition
Reason / 召回原因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 / 销售地区CO, NJ, England, South Africa,
Code information / 批次信息(a) lot IM445587, Exp 07/2019 (b) lot IM449808, Exp 07/2019
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Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.

Official record details

官方记录详情：以原始机构公告为准

Recall number / 召回编号

F-2150-2017

Classification / 风险等级

Medium / 中

Published / 发布时间

2017-05-03

Recalling firm / 召回企业

Armada Nutrition

Product description / 产品描述

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

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

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

Product quantity / 产品数量

1884 units

Distribution / 销售地区

CO, NJ, England, South Africa,

Reason for recall / 召回原因

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.

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Last synchronized: 2026-08-09. Recall Radar does not replace agency guidance.