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Lower risk Food recall · FDA · Published September 18, 2018

Purus Labs MYOWHEY Chocolate Cookie Crunch Protein Recall: Undeclared Milk and Soy

Purus Labs is recalling its MYOWHEY Premium Whey Protein, Chocolate Cookie Crunch due to undeclared milk and soy. Consumers should check product labels for the UPC 55734-00285 and contact the company for details.

🇺🇸 FDA recall #F-0005-2019FoodPurus Labs ›
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Recalling firmPurus Labs, Inc.2601 Resource Dr Ste 300 · Plano, TX 75074-8412
✎ GovInfoNow plain-language explainer

What happened, in plain English

Purus Labs is recalling its MYOWHEY Premium Whey Protein, Chocolate Cookie Crunch product because it contains undeclared milk and soy. This could cause allergic reactions in people with milk or soy allergies. The recall affects products sold with the UPC 55734-00285. Read more at govinfonow.com/recall/18663-purus-labs-myowhey-chocolate-cookie-crunch-protein-recall-undeclared-milk.

Source Summary by GovInfoNow · govinfonow.com/recall/18663-purus-labs-myowhey-chocolate-cookie-crunch-protein-recall-undeclared-milk · Updated October 6, 2026 · FDA enforcement record: FDA #F-0005-2019

Cite this page

“Purus Labs MYOWHEY Chocolate Cookie Crunch Protein Recall: Undeclared Milk and Soy.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18663-purus-labs-myowhey-chocolate-cookie-crunch-protein-recall-undeclared-milk. Based on FDA recall #F-0005-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0005-2019%22&limit=1).

Why it’s dangerous

The product contains undeclared milk and soy, which means it may cause allergic reactions in people who are sensitive to these ingredients. This is a food safety issue that could lead to allergic reactions if the person is allergic to milk or soy.

Who’s affected

People who have purchased this specific whey protein product with the UPC 55734-00285 are affected. Those with milk or soy allergies are at higher risk of allergic reactions.

How to tell if you have this one

Check the product label for the UPC 55734-00285. The product is a 5 lb / 2.26 kg whey protein powder with chocolate cookie crunch flavor.

  • Brand
    Purus Labs
  • Product
    Purus Labs MYOWHEY Premium Whey Protein, Chocolate Cookie Crunch, 75 True Servings, Net Wt. 5 lb / 2.26 kg. UPC
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 55734-00285 on the packaging to confirm if you have the recalled product.

Where it went and when

Where it was distributed

Distributed in 9 states, and outside the U.S.

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: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: yesCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “Within the US: AR, CT, FL, MI, NC, NV, OK, TX, VA. Outside the US: Chile and United Arab Emirates” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arkansas, Connecticut, Florida, Michigan, Nevada, North Carolina, Oklahoma, Texas, Virginia.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Sep 18, 201812. FDA classified it Class I: Oct 2, 201823. Published in FDA’s Enforcement Report: Oct 10, 201834. FDA terminated the recall: Feb 5, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class I
  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-0005-2019 (September 18, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0005-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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