RecallRadar
High RiskReported March 25, 2026

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

Recalled by Shaman Botanicals, LLC

Food recall

Shaman Botanicals, LLC

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

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 2 pack: 1281 units; 20-count: 14,491 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 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: Ko…”

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 had the active ingredient 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.

Full recall details

Status
Ongoing
Date reported
March 25, 2026
Recall started
February 13, 2026
Distributed in
MO
What was recalled
Product 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 …Show full text ▾Product 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
Why it was recalled (as stated by the FDA)
A sample of the product had the active ingredient in a quantity greater than the labeled specification.
How to identify the affected product
B#AAW.501.3; all expiration dates
Amount recalled
2 pack: 1281 units; 20-count: 14,491 units

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

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

According to the FDA: A sample of the product had the active ingredient in a quantity greater than the labeled specific…

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-1107-2026. Information last synced from the FDA on July 6, 2026.

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