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),…
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.
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.
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
| Type | Code / value | Context |
|---|---|---|
| UPC | 850043583608 | %) 120mg, (Providing 36mg Mitragynine), www.tyson20global.com, LGNDS, LLC, UPC: 850043583608, POWERED BY LGNDS, 12 bottles of 2oz each per case. |
| lot | U19231550 | Lot #U19231550, BEST BY: 11 JUL 24 |
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.