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Lower risk Food recall · FDA · Published March 12, 2026

Yunker Energy & Health Herbal Supplement with Vitamins Recall: Vitamin E Claim Not Met

Sato Pharmaceutical Inc. recalls Yunker Energy & Health Herbal Supplements due to not meeting Vitamin E label claims. Affected products include 30ml single servings with specific UPCs and expiration dates.

🇺🇸 FDA recall #H-0892-2026FoodYunker ›
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Recalling firmSato Pharmaceutical Inc.20695 S Western Ave Ste 240 · Torrance, CA 90501-1834
✎ GovInfoNow plain-language explainer

Sato Pharmaceutical Inc. is recalling Yunker Energy & Health Herbal Supplements with Vitamins because the product does not meet its label claim for Vitamin E. This means the supplement may not contain the advertised amount of Vitamin E, which could affect its nutritional value. Read more at govinfonow.com/recall/6655-yunker-energy-health-herbal-supplement-with-vitamins-recall-vitamin-e.

Source Summary by GovInfoNow · govinfonow.com/recall/6655-yunker-energy-health-herbal-supplement-with-vitamins-recall-vitamin-e · Updated August 10, 2026 · Official notice: FDA #H-0892-2026

Cite this page

“Yunker Energy & Health Herbal Supplement with Vitamins Recall: Vitamin E Claim Not Met.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/6655-yunker-energy-health-herbal-supplement-with-vitamins-recall-vitamin-e. Based on FDA recall #H-0892-2026.

The FDA announced on March 12, 2026, that Sato Pharmaceutical Inc. is recalling Yunker-branded Energy & Health Herbal Supplement with Vitamins because the product does not meet label claims for Vitamin E. The voluntary Class III recall affects 25,130 units distributed nationwide.

How to tell if you have it

  • Brand: Yunker
  • Product: Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml
  • UPCs: 49873-916-11, 49873-916-15, 49873-916-07, 00498739161510, 4987391607, 4987391611, 9873916113
  • Lot codes: CXW T, PXW Z, XXW W
  • Expiration dates: Jan-27, Mar-26, Dec-27

The hazard

The product does not meet label claims for Vitamin E. The FDA classified this as a Class III recall.

Context

GovInfoNow's records show Sato Pharmaceutical Inc. has three other recalls on file since February 16, 2017. On October 1, 2019, the firm recalled Zentrip 25mg Strips and Botanical Laxative Tablets due to subpotent drug risks. Other recent recalls of similar products include Pain Away Herbal Supplement Recall (November 20, 2025), Sinus Cap Herbal Supplement Recall (November 20, 2025), and A New Life Herbs Anti-virus Herbal Tincture Recall (November 20, 2025).

How to tell if you have this one

Check for the Yunker Energy & Health Herbal Supplement with Vitamins in 30ml containers. Look for the specific UPCs: 49873-916-11 (single), 49873-916-15 (3-pack), and 49873-916-07 (10-pack). Also check the expiration dates listed in the recall notice.

  • Brand
    Yunker
  • Product
    Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the product's UPC and expiration date to confirm if it matches the recalled items listed in the recall notice.

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: “Product was distributed to two domestic consignees who further distribute nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

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

1. Firm started the recall: Mar 12, 202612. FDA classified it Class III: Jun 2, 202623. Published in FDA’s Enforcement Report: Jun 10, 202632026
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report

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 #H-0892-2026 (March 12, 2026)
  • Plain-language summary written by qwen3:4b on August 10, 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