FDA recall H-1107-2026 · Mar 25, 2026
Shaman Botanicals, LLC: Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydr recall
Product
Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEMON DIETARY SUPPLEMENT Net Wt. 0.17 oz 10 PACKETS 2 TABLETS EACH Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed black flexible plastic bag with multi color sticker label on front and back UPC 810057763724
Reason for recall
A sample of the product had the active ingredient in a quantity greater than the labeled specification.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- B#AAW.501.3; all expiration dates
- Quantity
- 2 pack: 1281 units; 20-count: 14,491 units
- Distribution
- Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
- Recalling firm
- Shaman Botanicals, LLC, North Kansas City, MO
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-02-13
Source: openFDA enforcement record H-1107-2026 · search recall number H-1107-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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