Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg…

Shaman Botanicals, LLC recalled this product and the FDA reported the enforcement action on 25 March 2026 as Class I. The recall was initiated by the firm. A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product

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)

UPC

810057763779

Reason for recall

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

Recalling firm

Shaman Botanicals, LLC

Firm location

North Kansas City, Missouri, United States

Classification

Class I

Status

Ongoing

Recall number

H-1108-2026

Quantity

97,063 units

Distribution

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

Initiated

13 February 2026

Reported by FDA

25 March 2026

Firm notified by

Press Release

Product codes

B#AAW.501.3; all expiration dates

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

• Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
• The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
• This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 2 of them.
• This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
• The FDA published the enforcement report 6 weeks after the firm began the recall.
• Dietary supplements are regulated under their own good manufacturing practice rule, 21 CFR part 111, and they are the only food category where the dominant recall reason is an ingredient that was never declared because it is a pharmaceutical.

Filed under dietary supplements. A product can sit in more than one.

Other dietary supplements recalls

These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.

Other records from Shaman Botanicals, LLC

The FDA opens one enforcement record per product code, so several of these are frequently one recall event.

All 2026 recalls · All FDA food recall data