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Lower risk Food recall · FDA · Published February 13, 2017

World Organic Corp. Recalls Theravits 100 Vitamins Due to Missing Allergen Labels

World Organic Corp. recalls Theravits 100 and The Supreme One vitamins due to missing dietary ingredients on labels that may cause allergic reactions. All affected products were sold under multiple brand names.

🇺🇸 FDA recall #F-1544-2017FoodWorld Organic Corp. ›
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Recalling firmWorld Organic Corp.5242 Bolsa Ave., Ste. 3 · Huntington Beach, CA 92649-1054
✎ GovInfoNow plain-language explainer

What happened, in plain English

World Organic Corp. is recalling Theravits 100 and The Supreme One vitamins because they lack required dietary ingredients on their labels. This could cause allergic reactions for people sensitive to those ingredients. Read more at govinfonow.com/recall/22286-world-organic-corp-recalls-theravits-100-vitamins-due-to-missing.

Source Summary by GovInfoNow · govinfonow.com/recall/22286-world-organic-corp-recalls-theravits-100-vitamins-due-to-missing · Updated October 8, 2026 · FDA enforcement record: FDA #F-1544-2017

Cite this page

“World Organic Corp. Recalls Theravits 100 Vitamins Due to Missing Allergen Labels.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22286-world-organic-corp-recalls-theravits-100-vitamins-due-to-missing. Based on FDA recall #F-1544-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1544-2017%22&limit=1).

Why it’s dangerous

The vitamins contain dietary ingredients that are not listed on the product label, such as molybdenum, pancreatin, and others. These ingredients may cause allergic reactions in people sensitive to them.

Who’s affected

People who bought Theravits 100 or The Supreme One vitamins from stores like Clark's Nutrition or Hsu & Co. are most at risk if they have allergies to molybdenum, pancreatin, or other missing ingredients.

How to tell if you have this one

Check for Theravits 100 or The Supreme One vitamins with container sizes of 30, 60, 90, or 180. Product codes include 0783-30, 0786-60, 0789-90, 0788-180 for Theravits 100 and 680-030, 680-060, 680-090, 680-180 for The Supreme One.

  • Brand
    World Organic Corp.
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labels

    Look for the product code on the label to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed in 10 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: yesWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: 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: yesTXFlorida: not listedFL

FDA distribution: “US: WY, TX, VA, UT, ID, WA, OR, CA, OH, PA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Idaho, Ohio, Oregon, Pennsylvania, Texas, Utah, Virginia, Washington, Wyoming.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Feb 13, 201712. FDA classified it Class II: Feb 28, 201723. Published in FDA’s Enforcement Report: Mar 8, 201734. FDA terminated the recall: May 22, 201742017
  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-1544-2017 (February 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1544-2017 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