FDA Food EnforcementMedium / 中

Top Shelf White Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.

Recall F-1984-2018Published 2018-10-03Company Zakah Life LLC
Reason / 召回原因The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury. Also, based on FDA sample positive sample results, the red and green strains are potentially contaminated with Salmonella.
Distribution / 销售地区Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska
Code information / 批次信息TS050118, Exp: 06/2023
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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-1984-2018

Classification / 风险等级

Medium / 中

Published / 发布时间

2018-10-03

Recalling firm / 召回企业

Zakah Life LLC

Product description / 产品描述

Top Shelf White Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, packaged in 1) 90 capsules, 500 mg per capsules bottles, or 2) 3.52 oz // 100 grams of Kratom bags. Distributed by Zakah Life LLC Ankeny IA.

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

TS050118, Exp: 06/2023

Product quantity / 产品数量

10 100g bags

Distribution / 销售地区

Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska

Reason for recall / 召回原因

The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury. Also, based on FDA sample positive sample results, the red and green strains are potentially contaminated with Salmonella.

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