USPlabs recalls OxyELITE Pro Super Thermo Powder due to serious liver damage risk from Aegeline. Stop using if you have this 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.
USPl:abs is recalling its OxyELITE Pro Super Thermo Powder supplement because it contains Aegeline linked to serious liver damage or acute liver failure. This affects consumers who bought the product with the specific green apple flavor and 4.6 oz net weight.
The supplement contains Aegeline, which has been associated with serious liver damage or acute liver failure when taken. This risk is particularly concerning for individuals with pre-existing liver conditions or those taking medications that affect liver function.
People who own or use the USPlabs OxyELITE Pro Super Thermo Powder supplement with the green apple flavor and 4.6 oz net weight are affected. Those with liver conditions or taking medications that interact with liver function are at higher risk.
Check for the product name 'USPlabs OxyELITE Pro Super Thermo Powder Plus Advanced Carnitine Transport System' with green apple flavor and 4.6 oz net weight. The UPC code is 094922426499.
Immediately stop using the recalled supplement as it can cause serious liver damage or acute liver failure.
No, the product contains Aegeline linked to serious liver damage or acute liver failure, so it should not be used.
Stop using it immediately and contact USPlabs for further instructions.
Look for the product name 'USPlabs OxyELITE Pro Super Thermo Powder Plus Advanced Carnitine Transport System' with green apple flavor and 4.6 oz net weight, or check the UPC code 094922426499.
We’ve drafted a message you can send USPlabs to request your refund or repair — edit it as you like.
Subject: Recall F-1375-2014 — USPlabs USPlabs Hello, I own a USPlabs that is covered by recall F-1375-2014 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.
