USPlabs recalls OxyELITE Pro Super Thermo dietary supplements linked to serious liver damage or acute liver failure. Consumers should stop using affected products with specific UPC codes.
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 its OxyELITE Pro Super Thermo dietary supplements due to reports of serious liver damage and acute liver failure. This recall affects specific capsule sizes and UPC codes sold in the U.S.
The supplements contain Aegeline, which has been associated with serious liver damage and acute liver failure in users. This hazard occurs when the product is taken as directed without medical supervision.
People who purchased the recalled OxyELITE Pro Super Thermo dietary supplements in the U.S. are affected. Those with the specific UPC codes listed are most at risk.
Check the product label for the specific UPC codes listed: 094922417275 (2 count), 094922417251 (10 count), 094922417268 (10 count), 094922426604 (21 count), 094922395573 (90 count), 094922447906 (90 count 'Pink Label'), and 094922447852 (180 count).
Immediately stop using any recalled OxyELITE Pro Super Thermo dietary supplements with the listed UPC codes.
The supplements contain Aegeline, which has been linked to serious liver damage and acute liver failure.
The affected UPC codes are 094922417275 (2 count), 094922417251 (10 count), 094922417268 (10 count), 094922426604 (21 count), 094922395573 (90 count), 094922447906 (90 count 'Pink Label'), and 094922447852 (180 count).
Check the product label for the specific UPC codes listed in the recall notice.
We’ve drafted a message you can send USPlabs to request your refund or repair — edit it as you like.
Subject: Recall F-1370-2014 — USPlabs USPlabs Hello, I own a USPlabs that is covered by recall F-1370-2014 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.
