FDA recall, , High risk
Shaman Botanicals White Vein Advanced Alkaloids Chewable Tablets
White Vein Advanced Alkaloids Chewable Tablets contain more 7-Hydroxymitragynine than labeled, which could cause adverse health effects.
What happened
Shaman Botanicals, LLC, of North Kansas City, Missouri, recalled White Vein Advanced Alkaloids Chewable Tablets because a sample revealed the active ingredient 7-Hydroxymitragynine (7-OH) is present in a quantity greater than the labeled specification of 7.5 mg per tablet.
The affected products include the 225mg and 15mg versions, with the 225mg in white child-resistant plastic bottles and the 15mg in sealed silver metallic bags. The company began the recall on February 13, 2026, and the FDA added it to the Enforcement Report on March 13, 2026. The recall involved distribution to 14 wholesalers, 108 distributors, 46 company-owned stores, and 2202 online customers.
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What to do
If the UPC on your package is listed below:
- Wholesalers, distributors, retailers, and consumers that have the Alkaloids Chewable Tablets—White Vein product that is being recalled should quarantine the product, stop using it, and return it to Shaman Botanicals, LLC.
- Contact your physician or healthcare provider if you have experienced any problems that may be related to taking or using this dietary supplement product.
- To receive a full refund or replacement product, please go to the attached URL to register your return. https://recall.cbdamericanshaman.com/.
- Consumers with questions regarding this recall can contact Shaman Botanicals, LLC, Monday through Friday from 9am-5pm CST, at. Vince Sanders c/o Quality Department1501 Iron StreetNorth Kansas City, MO 64116Telephone: 855-427-7386Email: Quality@
CBDAmericanShaman.comhttps://recall.cbdamericanshaman.com/.
Is yours affected?
Affected if its UPC is listed.
The company's latest announcement of February 13, 2026 covers all expiration dates, so no lot or date is listed here.
A UPC is the number printed under a barcode.
Alkaloids Chewable Tablets, White Vein
- UPC
- 810057763724
- 810057763830
- 810057763779
Recall details
- Company began the recall
- Sold in
Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
- Company
- Shaman Botanicals, LLCNorth Kansas City, Missouri
- Hazard
- Labeling error
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98420
- Recall numbers
- H-1107-2026 to H-1108-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall · Announced by the company
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Listed on Recall Canary
Classified by FDA
Summary updated



