USPlabs is recalling OxyELITE Pro Super Thermo Powder due to serious liver damage or acute liver failure linked to Aegeline in the dietary supplement.
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 OxyEL:ITE Pro Super Thermo Powder supplement because it contains Aegeline, which has been linked to serious liver damage or acute liver failure. This recall is being handled by the FDA after receiving a voluntary recall notice.
The supplement contains Aegeline, a compound that has been associated with serious liver damage or acute liver failure when taken. This risk is particularly concerning for individuals with existing liver conditions or those who take higher doses.
People who own or use the OxyELITE Pro Super Thermo Powder supplement containing Aegeline are affected. Those with pre-existing liver conditions are at higher risk.
Look for the OxyELITE Pro Super Thermo Powder supplement with a blue raspberry flavor, 4.6 oz net weight, and UPC #094922426376. It was manufactured in Dallas, TX.
Immediately stop using the recalled OxyELITE Pro Super Thermo Powder supplement as it contains Aegeline linked to serious liver damage.
The supplement contains Aegeline, which has been linked to serious liver damage or acute liver failure.
Look for the OxyELITE Pro Super Thermo Powder with blue raspberry flavor, 4.6 oz net weight, and UPC #094922426376.
The recall notice does not specify a remedy, so you should stop using the product immediately.
We’ve drafted a message you can send USPlabs to request your refund or repair — edit it as you like.
Subject: Recall F-1373-2014 — USPlabs USPlabs Hello, I own a USPlabs that is covered by recall F-1373-2014 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.
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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.
