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Stop using now Food recall · FDA · Published November 23, 2016

Naturecom Recalls 500g DMAA Product for Undeclared Ingredient

Naturecom Inc. is recalling 500g DMAA products due to the presence of 1,3-dimethylamylamine. Check your silver and clear mylar bags.

🇺🇸 FDA recall #F-0762-2017FoodNaturecom ›
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Recalling firmNATURECOM INC8 Rancho Cir · Lake Forest, CA 92630-8325
✎ GovInfoNow plain-language explainer

What happened, in plain English

Naturecom Inc., doing business as NutriVitaShop, is recalling approximately 320kg of its 500g DMAA product because it may contain the undeclared ingredient 1,3-dimethylamylamine. The product was sold in silver and clear mylar ziplock bags with net weights of 500g. This recall affects units distributed nationwide in the US as well as internationally to countries including Canada, Australia, Great Britain, and others. Read more at govinfonow.com/recall/22815-naturecom-recalls-500g-dmaa-product-for-undeclared-ingredient.

Source Summary by GovInfoNow · govinfonow.com/recall/22815-naturecom-recalls-500g-dmaa-product-for-undeclared-ingredient · Updated October 11, 2026 · FDA enforcement record: FDA #F-0762-2017

Cite this page

“Naturecom Recalls 500g DMAA Product for Undeclared Ingredient.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/22815-naturecom-recalls-500g-dmaa-product-for-undeclared-ingredient. Based on FDA recall #F-0762-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0762-2017%22&limit=1).

Why it’s dangerous

The product may contain 1,3-dimethylamylamine, an ingredient that was not declared on the label. Undeclared pharmaceutical ingredients in supplements can pose serious health risks to consumers who are unaware they are consuming them.

Who’s affected

Consumers who purchased this specific 500g DMAA supplement from Naturecom/NutriVitaShop. Individuals who have ingested or plan to ingest the product are at risk due to the presence of undeclared ingredients.

How to tell if you have this one

Look for a silver and clear mylar ziplock bag containing approximately 500g of product. The manufacturer is Naturecom Inc. (dba NutriVitaShop). The record lists several date codes associated with the product: 20141102, 20150715, 20151022, 20160226, 20160701, 20161017, and 20150323.

  • Brand
    Naturecom
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using the Product

    Do not consume the product due to the potential presence of undeclared 1,3-dimethylamylamine.

  2. Check Packaging Details

    Verify if you have a silver and clear mylar ziplock bag containing 500g of product from Naturecom Inc.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in US & Worldwide: CA, AU, GB, ES, FR, AE, AT, BE, BG, CH, CL, CY, CZ, DE, DK, DO, FI, GI, GR, HR, HU, IE, IL, IT, JP, LT, LV, MT, MX, MY, NG, NL, NO, NZ, PH, PL, RE, RO, RU, SE, SG, SI, SK, TH, TR” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Nov 23, 201612. FDA classified it Class II: Dec 16, 201623. Published in FDA’s Enforcement Report: Dec 28, 201634. FDA terminated the recall: Jun 5, 2017420162017
  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-0762-2017 (November 23, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0762-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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