Armada Nutrition — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 22, 2026, Armada Nutrition has 7 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 23 Mar 2017. Armada Nutrition is categorized under Produce based on their predominant recall history.
Recall activity over time for Armada Nutrition
How serious are Armada Nutrition recalls?
FDA recall classifications by severity
Full FDA recall history for Armada Nutrition
All 7 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 23 Mar 2017Official FDA Notice | MP MUSCLEPHARM, ASSAULT, ENERGY + STRENGTH, THE ATHLETES PRE-WORKOUT, GREEN APPLE, 11.75 OZ (O.73 LBS) (333G), Exclusiv | A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation w | Class IITerminated |
| 23 Mar 2017Official FDA Notice | Muscle Meds(TM) PERFORMANCE TECHNOLOGIES, BIOENGINEERED BEEF PROTEIN ISOLATE CARNIVOR(TM) Dietary Supplement, Net Wt. 2 | A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation w | Class IITerminated |
| 23 Mar 2017Official FDA Notice | MYPROTEIN, MYPRE V2(TM) Net Wt. 17.6 Oz (1.1 lb) /500g, Blue Raspberry, preworkout, 500g, THE HUT GROUP(R), 1350 Cedar | A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation w | Class IITerminated |
| 23 Mar 2017Official FDA Notice | USN B4 -BOMB EXTREME PRE-WORKOUT, LIME LEMONADE FLAVOUR, 300g, USN North America, 1560 Sawgrass Corporation Pkwy, 4th F | A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation w | Class IITerminated |
| 23 Mar 2017Official FDA Notice | BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe | A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation w | Class IITerminated |
| 23 Mar 2017Official FDA Notice | PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, BLUE RAZZ ICE, NET WT 11.1 OZ (315G), Distributed by Performix LLC, 221 S | A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation w | Class IITerminated |
| 23 Mar 2017Official FDA Notice | PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, UNFLAVOURED, (a) 30 SERVINGS, UPC 8 11274 02239 8; (b) 45 SERVINGS, Distr | A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation w | Class IITerminated |
Where have Armada Nutrition recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
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