Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 23, 2017 (10 years ago)

Muscle Meds (TM) PERFORMANCE TECHNOLOGIES recall

Recalled by Armada Nutrition · Spring Hill, TN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

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.

Pathogen: Staphylococcus

Staph bacteria that can produce heat-stable toxins.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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

Quantity: 1884 units

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Colorado New Jersey

FDA's distribution note: CO, NJ, England, South Africa,

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Armada Nutrition
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 23, 2017
In FDA report of
May 3, 2017
Terminated
Feb 14, 2018
FDA recall number
F-2150-2017 · event 76825
Official record
FDA enforcement report search

Also recalled with it (6 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Staphylococcus

Myprotein Mypre V2

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…

Armada Nutrition CO, NJ F-2146-2017
Class II · Moderate risk Terminated Staphylococcus

Bulk Product Myprotein

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…

Armada Nutrition CO, NJ F-2147-2017
Class II · Moderate risk Terminated Staphylococcus

Performix (tm) Crea-Bead

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…

Armada Nutrition CO, NJ F-2148-2017
Class II · Moderate risk Terminated Staphylococcus

Usn B4 -Bomb Extreme Pre-Workout

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…

Armada Nutrition CO, NJ F-2149-2017
Class II · Moderate risk Terminated Staphylococcus

Mp Musclepharm Assault

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…

Armada Nutrition CO, NJ F-2151-2017
Class II · Moderate risk Terminated Staphylococcus

Performix (tm) Crea-Bead

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…

Armada Nutrition CO, NJ F-2152-2017

Recent dietary supplements recalls

All dietary supplements recalls