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Class I: serious health riskOngoing

Shaman Botanicals Product label reads in part as "WHITE VEIN Recall

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

Shaman Botanicals, LLC · North Kansas City, MO

Risk level
Class I
Reported by FDA
Mar 25, 2026
Recall ID
H-1108-2026
Check your lot numberHow we source this data

Summary

Shaman Botanicals recalled Product label reads in part as "WHITE VEIN starting Feb 13, 2026. The FDA classified it as Class I (serious health risk) and published enforcement report H-1108-2026 on Mar 25, 2026. Reason: A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification. Status: Ongoing.

Why it was recalled

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

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 numbers, UPCs & expiration codes

B#AAW.501.3; all expiration dates

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-1108-2026
Classification
Class I
Status
Ongoing
Recall initiated
Feb 13, 2026
FDA report date
Mar 25, 2026
Quantity
97,063 units
Recall type
Voluntary: Firm initiated
Recalling firm
Shaman Botanicals, LLC

Original FDA data

Every field from FDA enforcement report H-1108-2026, exactly as published.

Show all FDA fields
City
North Kansas City
State
MO
Status
Ongoing
Country
United States
Event ID
98420
Address
1501 Iron St
Code information
B#AAW.501.3; all expiration dates
Postal code
64116-3808
Report date
Mar 25, 2026
Product type
Food
Recall number
H-1108-2026
Classification
Class I
Recalling firm
Shaman Botanicals, LLC
Product quantity
97,063 units
Reason for recall
A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.
Voluntary / mandated
Voluntary: Firm initiated
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)
Distribution pattern
Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
Recall initiation date
Feb 13, 2026
Initial firm notification
Press Release
Center classification date
Jun 24, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-1108-2026, published Mar 25, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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