Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…

Shaman Botanicals, LLC has recalled Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 25, 2026 and was initiated on February 13, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…, with approximately 97,063 units affected. The company behind the recall is Shaman Botanicals, LLC, based in North Kansas City, MO. The FDA describes the product as: “Product 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:…”

Why was Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA… recalled?

According to the FDA, the stated reason for the recall is: “A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.”

What should you do?

If you think you may have bought Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…, compare it against the product description and identifying codes (B#AAW.501.3; all expiration dates) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Shaman Botanicals, LLC or your local health authority.

About this recall

This recall was distributed in MO. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.