FDA Recall: Advanced Alkaloids Alkaloids Chewable Tablets—White Vein
Source: FDA
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FDA Recall: Advanced Alkaloids Alkaloids Chewable Tablets—White Vein

Advanced Alkaloids February 18, 2026

FDA Recall: Advanced Alkaloids White Vein Chewable Tablets Contain Excess 7-Hydroxymitragynine

Shaman Botanicals, LLC is voluntarily recalling one lot of its Advanced Alkaloids White Vein chewable kratom tablets after independent tests showed more 7-Hydroxymitragynine (7-OH) than the 7.5 mg stated on the label. Consumers with the affected product should stop using it immediately and follow the company’s return instructions for a refund or replacement.

Key Recall Details

  • Recalled Product: Advanced Alkaloids White Vein Chewable Tablets (2-count, 20-count, 30-count)
  • Lot Number: B# AAW.501.3 (all expiration dates)
  • UPCs: 810057763724 (2-count), 810057763830 (20-count), 810057763779 (30-count)
  • Distribution: Nationwide (online, wholesalers, retailers)
  • Reason: Elevated 7-Hydroxymitragynine can increase overdose risk
  • Injuries Reported: None as of 17 Feb 2026
  • Announcement Date: 13 Feb 2026 (FDA posted 17 Feb 2026)

Sources

Why Are Advanced Alkaloids White Vein Tablets Being Recalled?

Lot B# AAW.501.3 exceeded the labeled 7.5 mg of 7-Hydroxymitragynine per tablet. Higher concentrations of this kratom alkaloid can cause stronger, unpredictable effects—ranging from nausea and dizziness to rapid heart rate or potentially severe complications in sensitive users.

Recommended Actions for Consumers

  • Verify the lot number (B# AAW.501.3) and matching UPCs on your package.
  • Discontinue use immediately if your product is affected.
  • Isolate the tablets so others cannot consume them accidentally.
  • Request a refund or replacement: complete the form at recall.cbdamericanshaman.com.
  • Seek medical advice if you experience adverse effects, and report them to FDA MedWatch.

Company Contact Information

Shaman Botanicals, LLC – Quality Department
1501 Iron Street, North Kansas City, MO 64116
Phone: 855-427-7386 (Mon–Fri, 9 am–5 pm CST)
Email: Quality@CBDAmericanShaman.com

Official Images from the Recall

Front label of Advanced Alkaloids White Vein chewable tablets
Source: FDA
Back label of Advanced Alkaloids White Vein chewable tablets
Source: FDA
Packaging of Advanced Alkaloids White Vein chewable tablets
Source: FDA

Frequently Asked Questions

Is my Advanced Alkaloids White Vein chewable tablet lot affected?

Only packages marked Lot B# AAW.501.3 with the specified UPC codes are recalled.

What health risks do Advanced Alkaloids White Vein Tablets pose when 7-Hydroxymitragynine is elevated?

Excess 7-OH can intensify kratom’s effects, leading to nausea, vomiting, rapid heartbeat, elevated blood pressure, or more serious reactions in sensitive individuals.

Can I continue using Advanced Alkaloids tablets from a different lot?

Yes. No other lots of Advanced Alkaloids White Vein tablets are part of this recall.

How do I get a refund or replacement for my Advanced Alkaloids White Vein tablets?

Visit recall.cbdamericanshaman.com, complete the form, and follow the emailed instructions to receive a prepaid shipping label and your choice of refund or replacement.

Did the FDA test Advanced Alkaloids White Vein chewable tablets before the recall?

The FDA is aware of the recall but has not indicated it performed its own laboratory analysis. The company initiated the recall based on independent third-party testing.

How should I dispose of recalled Advanced Alkaloids White Vein tablets?

Seal the tablets in a plastic bag with unpalatable waste (e.g., coffee grounds) and place them in household trash, or follow local drug-take-back guidelines. Do not flush them down the toilet.

Can retailers return unsold Advanced Alkaloids White Vein tablets from Lot B# AAW.501.3?

Yes. Retailers should quarantine affected inventory and contact the Quality Department at 855-427-7386 for return authorization and credit.

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