North Kansas City, MO (February 17, 2026) — The U.S. Food and Drug Administration (FDA) has announced a voluntary nationwide recall of Alkaloids Chewable Tablets—White Vein after tests showed the product contained higher-than-declared levels of 7-hydroxymitragynine (7-OH), an active alkaloid. According to the FDA, Shaman Botanicals, LLC initiated the recall due to the risk that consumers could ingest a stronger dose than intended.
Regulators said Shaman Botanicals sold the product nationwide through wholesalers, retailers, and online channels and has not received any reports of adverse events so far.
Shaman Botanicals recall: quick summary
The FDA confirmed that Shaman Botanicals recalled one lot of Alkaloids Chewable Tablets—White Vein after testing showed the product contained higher than the labeled 7.5 mg per tablet of 7-hydroxymitragynine. The company distributed the product nationwide in multiple package sizes. Company officials stated that consumers should stop using the tablets immediately and return them for a refund or replacement.
Official recall details
✦
Recall date: February 13, 2026 (FDA published February 17, 2026)
✦
Agency: U.S. Food and Drug Administration (FDA)
✦
Company: Shaman Botanicals, LLC
✦
Product: Alkaloids Chewable Tablets—White Vein (brand: Advanced Alkaloids)
✦
Issue: Undeclared higher concentration of 7-hydroxymitragynine (7-OH)
✦
Packaging: 2-count bag (UPC 810057763724), 20-count bag (UPC 810057763830), 30-count bottle (UPC 810057763779)
✦
Lot number: Lot B# AAW.501.3 (all expiration dates)
✦
Consumer action: Stop using the product and return it for a refund or replacement
✦
Stick around to find out more about this recall.
What happened?
The FDA said Shaman Botanicals initiated the recall after recent testing revealed that the tablets contained more 7-hydroxymitragynine than declared on the label. The company told regulators it became aware of the issue during internal quality testing. The recall was announced on February 13, 2026, in coordination with the FDA.
In its recall alert, the FDA warned that “use of the Alkaloids Chewable Tablets—White Vein product could result in consumers ingesting a higher dose than intended, which could result in adverse health effects.”
Affected products
Brand | Product | Size | UPC | Best by date | Issue | Distribution |
|---|---|---|---|---|---|---|
Advanced Alkaloids | Alkaloids Chewable Tablets—White Vein | 2-count bag | 810057763724 | All dates | Excess 7-OH | Nationwide |
Advanced Alkaloids | Alkaloids Chewable Tablets—White Vein | 20-count bag | 810057763830 | All dates | Excess 7-OH | Nationwide |
Advanced Alkaloids | Alkaloids Chewable Tablets—White Vein | 30-count bottle | 810057763779 | All dates | Excess 7-OH | Nationwide |
What caused the issue?
According to the FDA notice, the tablets contained more 7-hydroxymitragynine than stated on the label. This could expose users to a stronger dose than expected. Health risks may include nausea, dizziness, or other adverse reactions, particularly for individuals sensitive to alkaloid-based supplements. The agency confirmed that no illnesses have been reported to date.
Questions you might have
One lot of Alkaloids Chewable Tablets—White Vein with higher-than-declared 7-hydroxymitragynine levels.
Because consumers may ingest a stronger dose than intended, increasing health risks.
Lot B# AAW.501.3, across all expiration dates.
No adverse events have been reported to the FDA so far.
The company found it during recent product testing.
Nationwide through wholesalers, retailers, and online sales.
Stop using it immediately and return it for a refund or replacement.
Possible symptoms include nausea, dizziness, or other adverse reactions.
People sensitive to alkaloid-based supplements or those taking higher doses.
Shaman Botanicals’ Quality Department at 855-427-7386 or [email protected].
Here’s what you should do
- What to do with the product: Stop using it and return it for a refund or replacement.
- Where to look on the label: Check the lot number printed on the package or the bottom of the bottle.
- How to identify it: Lot B# AAW.501.3 in any package size.
- Brand contact: Vince Sanders, Quality Department, 855-427-7386, [email protected].
Behind the brand
Shaman Botanicals, LLC manufactures dietary supplement products sold under the Advanced Alkaloids name. The company’s recall notice states that it has “ceased distribution of the affected product” and is working closely with the FDA to ensure proper returns and refunds. Source86 reached out to Shaman Botanicals for additional comment, but has not yet received a response.
Other relevant recalls
Similar supplement and food recalls tied to undeclared or mismeasured active ingredients have surfaced in recent months, underscoring broader quality-control challenges across the industry. Recent cases include Initiative Foods, which recalled its Tippy Toes Apple Pear Banana product due to elevated patulin levels; Cargill, which issued a recall of Nutrena Country Feeds Cracked Corn for livestock over elevated aflatoxin levels; and Lucky Foods, which recalled cinnamon powder after testing revealed elevated lead concentrations. Together, these incidents highlight the ongoing risks associated with inaccurate testing, labeling, and batch verification in both the supplement and food supply chains.
“One of the major concerns with 7-hydroxymitragynine is that it acts as a powerful central nervous system depressant and carries a risk of dependence and withdrawal,” said Dr. Jamie Alan, Associate Professor of Pharmacology and Toxicology at Michigan State University. “Consumers may not realize how potent these compounds are, especially when product labeling does not accurately reflect the true dosage.”
Eran Mizrahi, CEO of Source86, added:
“Food safety isn’t just about compliance; it’s about trust. Every recall reminds us how vital it is to maintain transparency and rigorous checks.”
Ensuring safe eats
This recall underscores the importance of accurate labeling and consistent testing in the dietary supplement industry. Companies must strengthen quality assurance systems to prevent dosing errors, while consumers should always verify lot numbers and follow recall instructions.
At Source86, we help food and supplement brands manage sourcing and FSQA oversight with transparency and precision. Contact us.
