PlainRecalls
FDA Food Critical Class I Terminated

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.

Reported: October 3, 2018 Initiated: August 3, 2018 #F-1982-2018

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.

Reason for Recall

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.

Details

Recalling Firm
Zakah Life LLC
Units Affected
30 100g bags and 12 bottles and 8.4 kg of capsules
Distribution
Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska
Location
Ankeny, IA

Frequently Asked Questions

What product was recalled? ▼
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.. Recalled by Zakah Life LLC. Units affected: 30 100g bags and 12 bottles and 8.4 kg of capsules.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on October 3, 2018. Severity: Critical. Recall number: F-1982-2018.

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