Class I U.S. Food and Drug Administration

Advanced Alkaloids Alkaloids Chewable Tablets—White Vein recall: Product contains 7-Hydroxymitragynine (7-OH) in an amount more

Recall published 9 months ago

Product contains 7-Hydroxymitragynine (7-OH) in an amount more than the declared value of 7.5 mg/tablet.

Advanced Alkaloids Dietary supplements — recalled dietary supplementsAdvanced Alkaloids Dietary supplements — recalled dietary supplements (photo 2)Advanced Alkaloids Dietary supplements — recalled dietary supplements (photo 3)
3 photos published by U.S. Food and Drug Administration with the recall notice.

The hazard: Undeclared allergen or ingredient

The food itself is fine. What is wrong is the label, and for the households that rely on that label it is a real risk.

What the notice says: Risk Statement: 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.

Why it matters: An ingredient that U.S. law requires to be declared is present but missing from the label. People who avoid that ingredient cannot make a safe choice from the packaging.

Symptoms and when to call a doctor

An undeclared allergen is a danger only to people allergic or intolerant to that ingredient. For everyone else the food is safe. Reactions range from an itchy mouth, hives, stomach cramps or vomiting through to anaphylaxis — swelling of the lips, tongue or throat, a tight chest, wheezing, a sudden drop in blood pressure or collapse. If anaphylaxis is suspected, use an epinephrine auto-injector straight away and call 911, even if the symptoms seem to settle, because a second wave can follow hours later.

This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.

Recall details

Recall number
H-1107-2026, H-1108-2026
Published
February 13, 2026
Risk level
Class I
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Advanced Alkaloids
Product type
Dietary supplements
Units affected
2 pack: 1281 units; 20-count: 14,491 units; 97,063 units
Distribution
Nationwide
Lot / code info
B#AAW.501.3; all expiration dates
UPC codes
810057763724, 810057763830, 810057763779

Products covered by this recall

Alkaloids Chewable Tablets—White Vein

What the company announced

FOR IMMEDIATE RELEASE – February 13, 2026 – North Kansas City, Missouri, Shaman Botanicals, LLC is voluntarily recalling one lot (Lot B# AAW.501.3) of Alkaloids Chewable Tablets—White Vein to the consumer level. Recent testing showed that the Alkaloids Chewable Tablets—White Vein product contains 7-Hydroxymitragynine (7-OH) in an amount more than the declared value of 7.5 mg/tablet.

Risk Statement: 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.

Shaman Botanicals, LLC has not received any reports of adverse events related to this lot of Alkaloids Chewable Tablets—White Vein.

The product is packaged in a 2-count bag with UPC Code 810057763724, in a 20-count bag with UPC Code 810057763830 and in a 30-count bottle with UPC Code 810057763779. The affected Alkaloids Chewable Tablets—White Vein lot has the following lot number: Lot B# AAW.501.3 (all expiration dates). The product can be identified by the lot number on the package and/or the bottom of the bottle. The Alkaloids Chewable Tablets—White Vein product was distributed nationwide to wholesalers, retailers, and consumers via online sales.

Shaman Botanicals, LLC is notifying its distributors and customers by email and is arranging for return of the affected product and providing refunds or replacement of all recalled products. 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.

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 Department

1501 Iron Street

North Kansas City, MO 64116

Telephone: 855-427-7386

Email: [email protected]

https://recall.cbdamericanshaman.com/

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this dietary supplement product.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.

Complete and submit the report online: www.fda.gov/medwatch/report.htm

Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form or submit by fax to 1-800-FDA-0178.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Reproduced from the company announcement posted on fda.gov. Links and contact forms in the original are not repeated here; the official notice below has them.

Check your product

The notice names 15 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 810057763724
  • 810057763830
  • 810057763779

Model or item number

On the rating label, the box or the instruction sheet.

  • WY 828

Package size

Match the net weight or the piece count on the front of the pack.

  • 7.5 mg
  • 2 count
  • 20 count
  • 30 count
  • 15 mg
  • 0.02 oz
  • 150 mg
  • 0.17 oz
  • 2 pack
  • 225 mg
  • 0.25 oz

Codes are lifted verbatim from the FDA — Company recall announcements notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Allergen

Advanced Alkaloids — The food itself is fine. What is wrong is the label, and for the households that rely on that label it is a real risk.

  1. Read the official notice above for the exact ingredient involved, then check whether anyone in your home avoids it.
  2. If nobody here avoids it, the product is safe to eat; the refund is still available if you would rather return it.
  3. If someone does avoid it, stop serving it and check anything already cooked with it.
  4. Warn anyone else who eats from your kitchen, including schools and childminders.

Getting a refund without the pack

The commonest reason people skip the refund is that they have already thrown the item away. That rarely matters.

  • A photo of the label and lot code is accepted by most grocers, and so is a card statement line showing the purchase.
  • Store credit is often offered first. You can ask for the original payment method instead, and it is normally granted.
  • No photo either? Ask anyway. Grocery chains settle recall refunds at the service desk because disputing them costs more than paying them.
  • For a multi-pack or a case, ask for the full purchase price rather than a per-unit figure — the recall covers what you paid.

Remedy named in the notice: Shaman Botanicals, LLC is notifying its distributors and customers by email and is arranging for return of the affected product and providing refunds or replacement of all recalled products.

Company contact: Shaman Botanicals, LLC — Consumers: Vince Sanders, 855-427-7386, [email protected]

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Company recall announcements record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Advanced Alkaloids dietary supplements recalled?

Product contains 7-Hydroxymitragynine (7-OH) in an amount more than the declared value of 7.5 mg/tablet. Risk Statement: 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.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 810057763724, 810057763830, 810057763779; model number WY 828. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Read the official notice above for the exact ingredient involved, then check whether anyone in your home avoids it.

Can I get my money back?

The notice says: Shaman Botanicals, LLC is notifying its distributors and customers by email and is arranging for return of the affected product and providing refunds or replacement of all recalled products.

Where was the recalled product sold?

It was distributed nationwide.

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