Zakah Life LLC: 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.

Agency Publication Date: September 25, 2018

Affected Products

Product: Powerful Red Vein Bali 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.

SG010118, Exp: 06/2023

Product: Super Green 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.

SG50118, Exp: 06/2023

Product: 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.

TS050118, Exp: 06/2023

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 80729

Status: Resolved

Manufacturer: Zakah Life LLC

Manufactured In: United States

Units Affected: 3 products (30 100g bags and 12 bottles and 8.4 kg of capsules; 46 100g bags and 12 bottles and 8.4 kg of capsules.; 10 100g bags)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Affected Products

SG010118, Exp: 06/2023

SG50118, Exp: 06/2023

TS050118, Exp: 06/2023