USPlabs is recalling OxyELITE Pro Super Thermo Powder due to serious liver damage or acute liver failure linked to Aegeline in supplements. Consumers should stop using immediately.
USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse health events, namely serious liver damage or acute liver failure.
USPlabs is recalling their OxyELITE Pro Super Thermo Powder supplement because it contains Aegeline, which has been linked to serious liver damage and acute liver failure. This recall is urgent as the supplement poses a significant health risk.
The supplement contains Aegeline, a compound that has been associated with serious liver damage and acute liver failure when consumed. This risk is particularly concerning for individuals with liver conditions or those who take high doses of the supplement.
People who own or use the USPlabs OxyELITE Pro Super Thermo Powder supplement with the grape bubblegum flavor are affected. Those with pre-existing liver conditions are at higher risk.
Check for the product name 'USPlabs OxyELITE Pro Super Thermo Powder Plus Advanced Carnitine Transport System' with grape bubblegum flavor. The product was sold with a net weight of 4.6 oz (130 g) and has the UPC #094922447500.
Immediately stop using the recalled supplement as it can cause serious liver damage or acute liver failure.
USPlabs OxyELITE Pro Super Thermo Powder Plus Advanced Carnitine Transport System with grape bubblegum flavor, net weight 4.6 oz (130 g), UPC #094922447500.
The supplement contains Aegeline, which has been linked to serious liver damage and acute liver failure in some users.
Stop using it immediately and contact USPlabs for further instructions.
We’ve drafted a message you can send USPlabs to request your refund or repair — edit it as you like.
Subject: Recall F-1374-2014 — USPlabs USPlabs Hello, I own a USPlabs that is covered by recall F-1374-2014 from USPlabs. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
