USPlabs is recalling OxyELITE Pro Super Thermo Powder due to serious liver damage risks from Aegeline. Consumers should stop using and contact USPlabs for details.
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 dietary supplement because it contains Aegeline linked to serious liver damage. This affects consumers who have taken the product and may require medical attention.
The supplement contains Aegeline, which has been associated with serious liver damage and acute liver failure in some users. This risk occurs when the product is taken as directed, leading to potential health complications.
People who have taken USPlabs OxyELITE Pro Super Thermo Powder supplements are at risk of serious liver damage. Those who have consumed the product should stop using it immediately.
Check for the product name 'USPlabs OxyELITE Pro Super Thermo Powder Plus Advanced Carnitine Transport System' with a net weight of 4.6 oz (130 g) and the UPC #094922447494. The product was manufactured in Dallas, TX.
Immediately stop using the recalled OxyELITE Pro Super Thermo Powder supplement as it can cause serious liver damage.
The recalled product contains Aegeline, which has been linked to serious liver damage and acute liver failure.
Check for the product name 'USPlabs OxyELITE Pro Super Thermo Powder Plus Advanced Carnitine Transport System' with a net weight of 4.6 oz (130 g) and UPC #094922447494.
Stop using the product 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-1376-2014 — USPlabs USPlabs Hello, I own a USPlabs that is covered by recall F-1376-2014 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.
