Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS…
Reason A sample of the product had the active ingredient in a quantity greater than the labeled specification.
Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS… recall
Recalled by Shaman Botanicals, LLC · North Kansas City, MO, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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)
Quantity: 97,063 units
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
B#AAW.501.3; all expiration dates
Where it was sold
FDA's distribution note: Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall.
- Recalling firm
- Shaman Botanicals, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 13, 2026
- In FDA report of
- Mar 25, 2026
- FDA recall number
- H-1108-2026 · event 98420
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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