USPlabs recalls Fruit Punch dietary supplements due to risk of serious liver damage or acute liver failure. Products contain Aegeline and are linked to adverse health events. Check UPCs for affected items.
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 Fruit Punch dietary supplements because they contain Aegeline, which has been linked to serious liver damage or acute liver failure. This recall is based on FDA notifications of adverse health events.
The supplements contain Aegeline, a substance that has been associated with serious liver damage or acute liver failure. FDA reports indicate these adverse events occurred in users of the product.
People who own or use USPlabs Fruit Punch dietary supplements are affected. Those with pre-existing liver conditions may be at higher risk.
Check for UPC numbers: 094922417237, 094922447517, 094922426369, or 094922447487. The product comes in 0.15 oz, 4.6 oz, or 5 oz sizes.
Immediately stop using the recalled Fruit Punch dietary supplements as they contain Aegeline linked to serious liver damage.
USPlabs Fruit Punch dietary supplements with UPCs 094922417237, 094922447517, 094922426369, or 094922447487 in 0.15 oz, 4.6 oz, or 5 oz sizes.
The product contains Aegeline, which has been linked to serious liver damage or acute liver failure as reported by the FDA.
The recall record does not specify a remedy, but users 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-1372-2014 — USPlabs USPlabs Hello, I own a USPlabs that is covered by recall F-1372-2014 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.
