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Lower risk Food recall · FDA · Published March 23, 2017

MusclePharm Athletes Pre-Workout Recall: Staphylococcus aureus Risk

MusclePharm recalls Athletes Pre-Workout Green Apple flavor due to potential Staphylococcus aureus contamination from raw material testing failures.

🇺🇸 FDA recall #F-2151-2017FoodMusclePharm ›
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Recalling firmArmada Nutrition4637 Port Royal Rd · Spring Hill, TN 37174-2834
✎ GovInfoNow plain-language explainer

What happened, in plain English

MusclePharm is recalling their Athletes Pre-Workout Green Apple flavor because a raw material test initially failed for Staphylococcus aureus. This could mean the product might contain the bacterium that causes food poisoning. Consumers should check their product details and follow the official recall instructions. Read more at govinfonow.com/recall/21929-musclepharm-athletes-pre-workout-recall-staphylococcus-aureus-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/21929-musclepharm-athletes-pre-workout-recall-staphylococcus-aureus-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2151-2017

Cite this page

“MusclePharm Athletes Pre-Workout Recall: Staphylococcus aureus Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21929-musclepharm-athletes-pre-workout-recall-staphylococcus-aureus-risk. Based on FDA recall #F-2151-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2151-2017%22&limit=1).

Why it’s dangerous

The product was made using a raw material that initially failed Staphylococcus aureus testing. Although retesting passed, the investigation into why the initial test failed wasn't completed properly. This could mean the finished product contains the bacterium that causes food poisoning.

Who’s affected

Anyone who owns or uses MusclePharm's Athletes Pre-Workout Green Apple flavor (11.75 oz) is affected. People with weakened immune systems may be at higher risk from potential foodborne illness.

How to tell if you have this one

Check for the product name: MP MUSCLEPHARM, ASSAULT, ENERGY + STRENGTH, THE ATHLETES PRE-WORKOUT, GREEN APPLE, 11.75 OZ (0.73 LBS) (333G). The lot number IM448446 and expiration date 07/2018 are also on the label.

  • Brand
    MusclePharm
  • Product
    MP MUSCLEPHARM, ASSAULT, ENERGY + STRENGTH, THE ATHLETES PRE-WORKOUT, GREEN APPLE, 11.75 OZ (O.73 LBS) (333G)
  • Category
    Food
FDA recall event · 7 products

All 7 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    CO, NJ, England, South Africa,
Recall numberProduct, codes & lotsQuantity
F-2146-2017MYPROTEIN, 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; lot IM475137, Exp 01/20192,514 units
F-2147-2017BULK PRODUCT: MYPROTEIN, MYPRE Europe Base, bulk powder used for further processing in Europe; lot IM459653, Exp 08/2018 and lot IM470108, Exp 10/201839,600 kg
F-2148-2017PERFORMIX(TM) CREA-BEAD, MULTI-PHASE CREATINE, UNFLAVOURED, (a) 30 SERVINGS, UPC 8 11274 02239 8; (b) 45 SERVINGS, Distributed by Performix LLC, 221 S. Cherokee St., Denver, CO 80223, UPC 8 11274 02203 8; (a) lot IM458501, Exp 10/2018 (b) lot IM447128, Exp 07/2018, lot IM44551539,273 units
F-2149-2017USN B4 -BOMB EXTREME PRE-WORKOUT, LIME LEMONADE FLAVOUR, 300g, USN North America, 1560 Sawgrass Corporation Pkwy, 4th Floor, Sunrise, FL, 33323; lot IM453078, Exp 08/20183,997 units
F-2150-2017Muscle 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; (a) lot IM445587, Exp 07/2019 (b) lot IM449808, Exp 07/20191884 units
F-2151-2017MP 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 80239, UPC 6 53341 04601; lot IM448446, Exp 07/201814,496 units
F-2152-2017PERFORMIX(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; lot IM442915, Exp 08/201819,552 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name, lot number IM448446, and expiration date 07/2018 on the label.

Where it went and when

Where it was distributed

Distributed in Colorado and New Jersey.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “CO, NJ, England, South Africa,” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Colorado, New Jersey.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Mar 23, 201712. FDA classified it Class II: Apr 27, 201723. Published in FDA’s Enforcement Report: May 3, 201734. FDA terminated the recall: Feb 14, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-2151-2017 (March 23, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2151-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA