Shaman Botanicals, LLC Issues Voluntary Nationwide Recall of Alkaloids Chewable Tablets—White Vein Due to Undeclared Concentration of 7-Hydroxymitragynine (7-OH)

Tue Feb 17 2026

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Dietary Supplements

Reason for Recall

Product contains 7-Hydroxymitragynine (7-OH) in an amount more than the declared value of 7.5 mg/tablet.

Product Information:

Brand	Company	Product Description
Advanced Alkaloids	Shaman Botanicals, LLC	Alkaloids Chewable Tablets—White Vein

Company Announcement

FOR IMMEDIATE RELEASE – February 13, 2026 – North Kansas City, Missouri, Shaman Botanicals, LLC is voluntarily recalling one lot (Lot B# AAW.501.3) of Alkaloids Chewable Tablets—White Vein to the consumer level. Recent testing showed that the Alkaloids Chewable Tablets—White Vein product contains 7-Hydroxymitragynine (7-OH) in an amount more than the declared value of 7.5 mg/tablet.

Risk Statement: Use of the Alkaloids Chewable Tablets—White Vein product could result in consumers ingesting a higher dose than intended, which could result in adverse health effects.

Shaman Botanicals, LLC has not received any reports of adverse events related to this lot of Alkaloids Chewable Tablets—White Vein.

The product is packaged in a 2-count bag with UPC Code 810057763724, in a 20-count bag with UPC Code 810057763830 and in a 30-count bottle with UPC Code 810057763779. The affected Alkaloids Chewable Tablets—White Vein lot has the following lot number: Lot B# AAW.501.3 (all expiration dates). The product can be identified by the lot number on the package and/or the bottom of the bottle. The Alkaloids Chewable Tablets—White Vein product was distributed nationwide to wholesalers, retailers, and consumers via online sales.

Shaman Botanicals, LLC is notifying its distributors and customers by email and is arranging for return of the affected product and providing refunds or replacement of all recalled products. Wholesalers, distributors, retailers, and consumers that have the Alkaloids Chewable Tablets—White Vein product that is being recalled should quarantine the product, stop using it, and return it to Shaman Botanicals, LLC.

To receive a full refund or replacement product, please go to the attached URL to register your return. https://recall.cbdamericanshaman.com/.

Consumers with questions regarding this recall can contact Shaman Botanicals, LLC, Monday through Friday from 9am-5pm CST, at:

Vince Sanders c/o Quality Department
1501 Iron Street
North Kansas City, MO 64116
Telephone: 855-427-7386
Email: Quality@CBDAmericanShaman.com
https://recall.cbdamericanshaman.com/

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this dietary supplement product.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.

• Complete and submit the report online: www.fda.gov/medwatch/report.htm
• Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form or submit by fax to 1-800-FDA-0178.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Published Documents:

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