Check the Batch
Class IITerminated in FDA datasetRecall initiated Oct 13, 2023

TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, Mocha, 2oz (60ml), Supplement Facts, Kava Root…

Recalling firm: LGNDS LLC

Why it was recalled

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.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 25, 2024.

Check your package

Compare the exact product and package details with the label you have.

ProductTYSON 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.
Package size2oz
UPC850043583608

FDA code information

Lot #U19231550, BEST BY: 11 JUL 24

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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.

Extracted codes and context

TypeCode / valueContext
UPC850043583608%) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583608, POWERED BY LGNDS, 12 bottles of 2oz each per case.
lotU19231550Lot #U19231550, BEST BY: 11 JUL 24

Original FDA recall 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.

Recall details

Recall number
F-0504-2024
Event ID
93371
FDA status
Terminated
Initiated
Oct 13, 2023
Reported
Dec 20, 2023
Classified
Dec 8, 2023
Terminated
Jan 25, 2024
Quantity
15,000 units of 2oz each
Location
Miami, FL, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

U.S. distribution only.

FDA source record · F-0504-2024

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.