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Stop using now Food recall · FDA · Published February 13, 2026

Shaman Botanicals Recalls White Vein Chewable Tablets Due to Dosage Error

Shaman Botanicals recalls White Vein Advanced Alkaloids chewable tablets because the active ingredient exceeds labeled amounts. Check your bottle now.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-1108-2026FoodShaman Botanicals ›
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Contact the company

Recalling firmShaman Botanicals, LLC1501 Iron St · North Kansas City, MO 64116-3808
✎ GovInfoNow plain-language explainer

Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because a sample revealed the active ingredient is present in a quantity greater than what is listed on the label. This product was distributed to wholesalers, distributors, company-owned stores, and online customers. The recall covers 97,063 units with all expiration dates. Read more at govinfonow.com/recall/6739-shaman-botanicals-recalls-white-vein-chewable-tablets-due-to-dosage.

Source Summary by GovInfoNow · govinfonow.com/recall/6739-shaman-botanicals-recalls-white-vein-chewable-tablets-due-to-dosage · Updated October 9, 2026 · Official notice: FDA #H-1108-2026

Cite this page

“Shaman Botanicals Recalls White Vein Chewable Tablets Due to Dosage Error.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6739-shaman-botanicals-recalls-white-vein-chewable-tablets-due-to-dosage. Based on FDA recall #H-1108-2026.

Shaman Botanicals, LLC voluntarily recalled White Vein Advanced Alkaloids Chewable Tablets on Feb. 13, 2026, after samples revealed the active ingredient exceeded labeled specifications, according to the FDA. Owners should stop using the product immediately.

How to tell if you have it

  • Brand: Shaman Botanicals
  • Product: White Vein Advanced Alkaloids Chewable Tablets
  • Label text: WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS
  • Manufacturer: Konig Products, LLC
  • UPC: 810057763779 (sometimes preceded by 00)
  • B#: AAW.501.3
  • Expiration dates: all
  • Units affected: 97,063

The hazard

A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

Context

GovInfoNow's records show other recent recalls of similar products include A New Life Herbs Anti-virus Herbal Tincture Recall (2025-11-20), Sinus Cap Herbal Supplement Recall (2025-11-20), and Wild Coast Brew Tart Chocolaty Tisane Recall (2026-06-05).

How to tell if you have this one

Look for a white child-resistant plastic bottle with a sticker label reading "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container". Check for UPC 810057763779 (sometimes preceded by 00), B#AAW.501.3, and any expiration date.

  • Brand
    Shaman Botanicals
  • Product
    Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Ongoing
  • Distribution
    Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
Recall numberProduct, codes & lotsQuantity
H-1107-2026Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEMON DIETARY SUPPLEMENT Net Wt. 0.17 oz 10 PACKETS 2 TABLETS EACH Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed black flexible plastic bag with multi color sticker label on front and back UPC 810057763724; B#AAW.501.3; all expiration dates2 pack: 1281 units; 20-count: 14,491 units
H-1108-2026Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: White child-resistant plastic bottle with sticker label applied UPC 810057763779 (sometimes proceeded by 00); B#AAW.501.3; all expiration dates97,063 units
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume the tablets as the active ingredient amount exceeds the labeled specification.

  2. Check your bottle details

    Verify if you have the recalled item by checking for UPC 810057763779, B#AAW.501.3, and the specific label text.

  3. Contact the manufacturer

    Reach out to Shaman Botanicals, LLC for further instructions on the remedy.

How this recall unfolded

Recall timeline

FDA published this recall 40 days after the firm started it.

1. Firm started the recall: Feb 13, 202612. Published in FDA’s Enforcement Report: Mar 25, 202623. FDA classified it Class I: Jun 24, 202632026
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I

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-1108-2026 (February 13, 2026)
  • 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