Drug recall

BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe

FDA recall event 76825 · Class II · Armada Nutrition

Key facts

Event ID 76825
Recall numbers F-2146-2017, F-2147-2017, F-2148-2017, F-2149-2017, F-2150-2017, F-2151-2017, F-2152-2017
Recalling firm Armada Nutrition
Product type Food
Products BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe, MP MUSCLEPHARM, ASSAULT, ENERGY + STRENGTH, THE ATHLETES PRE-WORKOUT, GREEN APPLE, 11.75 OZ (O.73 LBS) (333G), Exclusively Developed & Manufactured for: MusclePharm Corp., 721 Ironton St., Denver, CO…, 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…, MYPROTEIN, MYPRE V2(TM) Net Wt. 17.6 Oz (1.1 lb) /500g, Blue Raspberry, preworkout, 500g, THE HUT GROUP(R), 1350 Cedar Grove Park, Shepherdsville, KY, UPC 5 065104 570111, PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, BLUE RAZZ ICE, NET WT 11.1 OZ (315G), Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02204 5 and 2 more
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
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…
Initiation date Mar 23, 2017
Report date May 3, 2017
Termination date Feb 14, 2018
City Spring Hill
State TN
Country United States
FEI number 3012501275

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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