RecallHawk
Class I Recall

Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container

Shaman Botanicals, LLC

Summary

The FDA issued a Class I for Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 2 by Shaman Botanicals, LLC. Reason: A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification..

Details

Source

Food Recall

External ID

H-1108-2026

Action Date

2026-03-25

Status

Ongoing

Category

food

Product Description

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: 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)

Lot/Code Info: B#AAW.501.3; all expiration dates

Quantity Affected: 97,063 units

Reason for Recall

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

Distribution

Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers

Type: Voluntary: Firm initiated

Recall Initiated: 2026-02-13

Company

Shaman Botanicals, LLC

North Kansas City, MO

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Shaman Botanicals, LLC has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Shaman Botanicals, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Shaman Botanicals, LLC have FDA actions?

Shaman Botanicals, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1108-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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