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Recall Radar/FDA Food Enforcement/F-1376-2014

FDA Food EnforcementHigh / 高

USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport System DIETARY SUPPLEMENT Net Wt. 4.6 oz (130 g) RASPBERRY LEMONADE Manufactured for USPlabs, LLC (Dallas, TX 75220)

Recall F-1376-2014Published 2014-01-22Company USPlabs, LLC
Reason / 召回原因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.
Distribution / 销售地区Worldwide distribution including the following Worldwide distribution including the following international countries: Ecuador, Russia, UAE, South America, Dominican Republic, Kuwait, Philippines, Indonesia, Egypt, Panama, China, and Argentina.
Code information / 批次信息UPC #094922447494
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Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.

Official record details

官方记录详情：以原始机构公告为准

Recall number / 召回编号

F-1376-2014

Classification / 风险等级

High / 高

Published / 发布时间

2014-01-22

Recalling firm / 召回企业

USPlabs, LLC

Product description / 产品描述

USPlabs OxyELITE Pro Super Thermo POWDER Plus Advanced Carnitine Transport System DIETARY SUPPLEMENT Net Wt. 4.6 oz (130 g) RASPBERRY LEMONADE Manufactured for USPlabs, LLC (Dallas, TX 75220)

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

UPC #094922447494

Product quantity / 产品数量

10,278 units

Distribution / 销售地区

Worldwide distribution including the following Worldwide distribution including the following international countries: Ecuador, Russia, UAE, South America, Dominican Republic, Kuwait, Philippines, Indonesia, Egypt, Panama, China, and Argentina.

Reason for recall / 召回原因

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.

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Last synchronized: 2026-08-09. Recall Radar does not replace agency guidance.