---
title: "TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, Mocha, 2oz (60ml), Supplement Fac... — FDA record F-0504-2024 | Is It on Recall"
description: "Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot ex"
url: https://isitonrecall.com/recall/fda-food-f-0504-2024-tyson-2-0-tyson-tonic-kava-kratom-blend-mocha-2oz-60ml-supplement-facts-kava-root-extract-30-1200mg/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, Mocha, 2oz (60ml), Supplement Facts, Kava Root Extract (30%) 1200mg, Krat... — FDA record F-0504-2024

Reported terminated

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 Oct 13, 2023. 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**: TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, Mocha, 2oz (60ml), Supplement Facts, Kava Root Extract (30%) 1200mg, Kratom Leaf Extract (30%) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583608, POWERED BY LGNDS, 12 bottles of 2oz each per case.
- **Reason**: Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.
- **Classification**: Class II
- **Recalling firm**: LGNDS LLC
- **Quantity**: 15,000 units of 2oz each
- **Agency-reported status**: Terminated
- **Source record identifier**: F-0504-2024

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0504-2024%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 | Lot #U19231550, BEST BY: 11 JUL 24 |

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

## Distribution

U.S. distribution only.

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

## Dates in the source

- **Report date**: Dec 20, 2023
- **Recall initiation date**: Oct 13, 2023
- **Center classification date**: Dec 8, 2023
- **Termination date**: Jan 25, 2024

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%22F-0504-2024%22)

## Related records

[Other food records](https://isitonrecall.com/category/other-food/) [LGNDS LLC records](https://isitonrecall.com/brand/lgnds-llc/)