USPlabs recalls OxyELITE Pro dietary supplements due to risk of serious liver damage or acute liver failure. Affected products include 3-count, 90-count, and 180-count capsules with specific UPCs.
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 dietary supplements after FDA reports serious liver damage or acute liver failure linked to products containing Aegeline. Consumers should stop using these supplements immediately.
The supplement contains Aegeline, which has been linked to serious liver damage and acute liver failure in some users. This occurs when the substance is metabolized by the body in a way that causes harm to liver tissue.
Anyone who owns or uses USPlabs OxyELITE Pro supplements with the listed UPC codes. People with pre-existing liver conditions are at higher risk.
Check for 3-count, 90-count, or 180-count capsules with UPC numbers: 094922447883, 094922447876, 094922395627, or 094922447869. These were sold in the United States.
Immediately stop using all recalled OxyELITE Pro supplements as they can cause serious liver damage.
The supplements contain Aegeline, which has been linked to serious liver damage or acute liver failure in some users.
Affected UPCs are 094922447883, 094922447876, 094922395627, and 094922447869.
Look for 3-count, 90-count, or 180-count capsules with the listed UPC numbers. These were sold in the United States.
We’ve drafted a message you can send USPlabs to request your refund or repair — edit it as you like.
Subject: Recall F-1371-2014 — USPlabs USPlabs Hello, I own a USPlabs that is covered by recall F-1371-2014 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.
