FDA Food EnforcementMedium / 中

TruBoost Drink - Citrine Spark

Recall F-0950-2023Published 2023-05-31Company TruVision Health LLC
Reason / 召回原因The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Distribution / 销售地区Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Code information / 批次信息Lot PM17921F1
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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-0950-2023

Classification / 风险等级

Medium / 中

Published / 发布时间

2023-05-31

Recalling firm / 召回企业

TruVision Health LLC

Product description / 产品描述

TruBoost Drink - Citrine Spark

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

Lot PM17921F1

Product quantity / 产品数量

1,789 packs

Distribution / 销售地区

Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand

Reason for recall / 召回原因

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

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