LGNDS LLC recalls Tyson 2.0 and Kava-Kratom blends due to unapproved kratom and high pH levels. Consumers should check product labels for lot #U19231550.
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.
LGNDS LLC is recalling Tyson 2.0 and Kava-Kratom blends because they contain kratom, an unapproved food additive, and have a pH level above 5.0. This could pose risks if consumed as a food product.
The product contains kratom, which is not approved as a food additive, and has a pH level over 5.0. The process requires the product to be acidified with a pH below 3.30, but this product does not meet that standard.
Anyone who purchased the Tyson 2.0, Tyson Tonic Kava & Kratom Blend, or Mocha flavors from LGNDS LLC. People using these products for food purposes are most at risk.
Check for the product name 'Tyson 2.0', 'Tyson Tonic Kava & Kratom Blend', or 'Mocha' on the label. Look for lot number U19231550 and the best by date of July 11, 2024.
Look for the lot number U19231550 and best by date of July 11, 2024 on the label.
The product contains kratom, an unapproved food additive, and has a pH level above 5.0, which may not be safe for consumption as a food product.
The recall does not specify a remedy, so check the product label for the lot number and best by date to determine if it's affected.
The product contains kratom, which is not approved as a food additive, and has a pH level over 5.0, which does not meet the required acidification standard.
We’ve drafted a message you can send Tyson to request your refund or repair — edit it as you like.
Subject: Recall F-0504-2024 — Tyson Tyson Hello, I own a Tyson that is covered by recall F-0504-2024 from Tyson. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.