---
title: "Product label reads in part as \"WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLET... — FDA record H-1107-2026 | Is It on Recall"
description: "A sample of the product had the active ingredient in a quantity greater than the labeled specification."
url: https://isitonrecall.com/recall/fda-food-h-1107-2026-product-label-reads-in-part-as-white-vein-advanced-alkaloids-chewable-tablets-15mg-7-hydroxymitragyn/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per containe... — FDA record H-1107-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 13, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: A sample of the product had the active ingredient in a quantity greater than the labeled specification.
- **Classification**: Class I
- **Recalling firm**: Shaman Botanicals, LLC
- **Quantity**: 2 pack: 1281 units; 20-count: 14,491 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: H-1107-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1107-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | B#AAW.501.3; all expiration dates |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Mar 25, 2026
- **Recall initiation date**: Feb 13, 2026
- **Center classification date**: Jun 24, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1107-2026%22)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [Shaman Botanicals, LLC records](https://isitonrecall.com/brand/shaman-botanicals-llc/)