Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…
Recalled by Shaman Botanicals, LLC
Food recall
Shaman Botanicals, LLC
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
Shaman Botanicals, LLC has recalled Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 25, 2026 and was initiated on February 13, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…, with approximately 97,063 units affected. The company behind the recall is Shaman Botanicals, LLC, based in North Kansas City, MO. The FDA describes the product as: “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:…”
Why was Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA… recalled?
According to the FDA, the stated reason for the recall is: “A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.”
What should you do?
If you think you may have bought Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…, compare it against the product description and identifying codes (B#AAW.501.3; all expiration dates) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Shaman Botanicals, LLC or your local health authority.
About this recall
This recall was distributed in MO. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Who this recall affects
This recall matters to anyone who bought Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.
Distribution listed in the notice: Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: B#AAW.501.3; all expiration dates
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact Shaman Botanicals, LLC or your local health department.
Full recall details
- Status
- Ongoing
- Date reported
- March 25, 2026
- Recall started
- February 13, 2026
- Distributed in
- MO
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…Show full text ▾
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)What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA… recalled?+
According to the FDA: A sample of the product revealed the active ingredient is in a quantity greater than the labeled…
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWA…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-1108-2026. Information last synced from the FDA on October 9, 2026.