H-1107-2026
Shaman Botanicals, LLC
Data retrieved 2026-10-27T22:06:49.008Z
Site-assigned category (for this product recall): Potency/formulation
Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.
Official openFDA record · FDA recalls and safety alerts
Fields as reported by FDA
Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.
- recall_number
- H-1107-2026
- event_id
- 98420
- recalling_firm
- Shaman Botanicals, LLC
- city
- North Kansas City
- state
- MO
- country
- United States
- product_description
- 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.
- classification
- Class I
- FDA-reported status (not current status)
- Ongoing
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated. - voluntary_mandated
- Voluntary: Firm initiated
- distribution_pattern
- Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
- product_quantity
- 2 pack: 1281 units; 20-count: 14,491 units
- code_info
- B#AAW.501.3; all expiration dates
- recall_initiation_date
- 2026-02-13
- report_date
- 2026-03-25
- termination_date
- Not reported