CLASS I Food recall · Reported 3 Oct 2018 · FDA Enforcement Report

Super Green Maeng Da Premium Kratom recalled by Zakah Life

Zakah Life is recalling Super Green Maeng Da Premium Kratom, Zakah Life Dietary Supplement, Mitragyn Speciosa, distributed in Colorado, Iowa, Illinois, Nebraska. The recall was initiated on 3 Aug 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSG50118, Exp: 06/2023
Quantity recalled46 100g bags and 12 bottles and 8.4 kg of capsules.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1983-2018
FDA event ID
80729
Recalling firm
Zakah Life, Ankeny, IA
Brand
Super
Classification
Class I
Status
Terminated
Recall initiated
3 Aug 2018
FDA classified
25 Sep 2018
Reported
3 Oct 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Energy Drinks

Timeline

3 Aug 2018Recall initiated by company
25 Sep 2018Classified by FDA+53 days
3 Oct 2018Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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.

Where it was distributed

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

ColoradoIowaIllinoisNebraska

Questions about this recall

Why was it 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 lots are affected?

SG50118, Exp: 06/2023

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 80729

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FoodCLASS IPowerful Red Vein Bali Premium Kratom recalled by Zakah LifePowerfulZakah LifeSalmonella4 states

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