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

Recall: Michael's Cholesterol Metabolism Factors due to undeclared allergens

Inner Health Group recalls Cholesterol Metabolism Factors tablets for containing undeclared milk and soy. Check lot numbers if you have these supplements.

🇺🇸 FDA recall #F-1869-2016FoodMichael's Naturopathic Programs ›
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Recalling firmInner Health Group, Inc dba Michael's Naturopathic Programs6003 Randolph Blvd. · San Antonio, TX 78233
✎ GovInfoNow plain-language explainer

What happened, in plain English

Inner Health Group, Inc., doing business as Michael's Naturopathic Programs, is recalling Cholesterol Metabolism Factors tablets in 270, 180, and 90 count sizes. The products may contain undeclared milk (calcium caseinate) and soy, which poses a risk to individuals with allergies to these ingredients. The recall covers specific lots distributed nationwide. Read more at govinfonow.com/recall/23917-recall-michael-s-cholesterol-metabolism-factors-due-to-undeclared-allergens.

Source Summary by GovInfoNow · govinfonow.com/recall/23917-recall-michael-s-cholesterol-metabolism-factors-due-to-undeclared-allergens · Updated October 9, 2026 · FDA enforcement record: FDA #F-1869-2016

Cite this page

“Recall: Michael's Cholesterol Metabolism Factors due to undeclared allergens.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23917-recall-michael-s-cholesterol-metabolism-factors-due-to-undeclared-allergens. Based on FDA recall #F-1869-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1869-2016%22&limit=1).

Why it’s dangerous

The tablets may contain undeclared milk and soy allergens. For people with sensitivities or allergies to these ingredients, accidental ingestion can trigger serious allergic reactions.

Who’s affected

Consumers who purchased Michael's Naturopathic Programs Cholesterol Metabolism Factors tablets in plastic bottles. Individuals with milk or soy allergies are at the highest risk of an allergic reaction.

How to tell if you have this one

Check your plastic bottles for the product name 'Cholesterol Metabolism Factors' in 270, 180, or 90 count sizes. Verify the lot number on the label against this list: 1307013, 1310060, 1402177, 1405356, 1408114, 1410186, 1501476, 1505367, 1510296, 1602062.

  • Brand
    Michael's Naturopathic Programs
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled tablets if you have any of the listed lot numbers.

  2. Check your bottle label

    Look for the specific lot numbers to confirm if your product is part of this recall.

Where it went and when

Where it was distributed

Distributed nationwide.

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” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

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

1. Firm started the recall: Jun 23, 201612. FDA classified it Class I: Aug 3, 201623. Published in FDA’s Enforcement Report: Aug 10, 201634. FDA terminated the recall: Dec 16, 201642016
  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-1869-2016 (June 23, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1869-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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