LGNDS LLC recalls Tyson 2.0 and related supplements due to unapproved kratom and incorrect pH levels. Consumers should check product labels for lot numbers and contact the company for details.
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, Tyson Tonic Kava & Kratom Blend, and Fruit Punch supplements because they contain kratom, an unapproved food additive, and have a pH level above 3.30. This could pose a risk to consumers if the product is consumed.
The product contains kratom, which is not approved as a food additive by regulatory authorities. Additionally, the pH level of the product exceeds the safe limit of 3.30, which could affect stability and safety.
Anyone who purchased the Tyson 2.0, Tyson Tonic Kava & Kratom Blend, or Fruit Punch supplements from LGNDS LLC. People using these products for health purposes may be at risk due to the unapproved kratom content.
Check for the product name 'Tyson 2.0', 'Tyson Tonic Kava & Kratom Blend', or 'Fruit Punch' on the label. Look for the lot number U20231558 and the best by date of July 21, 2024.
Look for the lot number U20231558 and best by date of July 21, 2024 on the product label.
The product contains kratom, an unapproved food additive, and has a pH level above 3.30, which may pose a risk. Consumers should check if they have the recalled product and follow the recall instructions.
Check for the product name 'Tyson 2.0', 'Tyson Tonic Kava & Kratom Blend', or 'Fruit Punch' on the label with lot number U20231558 and best by date of July 21, 2024.
The recall record does not specify a remedy, so consumers should check the product label and contact LGNDS LLC for further instructions.
We’ve drafted a message you can send Tyson to request your refund or repair — edit it as you like.
Subject: Recall F-0505-2024 — Tyson Tyson Hello, I own a Tyson that is covered by recall F-0505-2024 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.
