Class ITerminated in FDA datasetRecall initiated Aug 3, 2018

Powerful Red Vein Bali Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa,…

Recalling firm: Zakah Life LLC

Why it was recalled

The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with inadequate information to provide reasonable assurance that such…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 26, 2018.

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ProductPowerful 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.
Package size3.52 oz

FDA code information

SG010118, Exp: 06/2023

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Full FDA record and distribution details

Original product description

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.

Original FDA recall reason

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.

Recall details

Recall number
F-1982-2018
Event ID
80729
FDA status
Terminated
Initiated
Aug 3, 2018
Reported
Oct 3, 2018
Classified
Sep 25, 2018
Terminated
Oct 26, 2018
Quantity
30 100g bags and 12 bottles and 8.4 kg of capsules
Location
Ankeny, IA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

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

FDA source record · F-1982-2018

Data updated September 16, 2026. View official FDA data ↗

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