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Class I: serious health riskTerminated

Zakah Life Powerful Red Vein Bali Premium Kratom Recall

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

Zakah Life LLC · Ankeny, IA

Risk level
Class I
Reported by FDA
Oct 3, 2018
Recall ID
F-1982-2018
Check your lot numberHow we source this data

Summary

Zakah Life recalled Powerful Red Vein Bali Premium Kratom starting Aug 3, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-1982-2018 on Oct 3, 2018. 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. Status: Terminated.

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 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.

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.

Lot numbers, UPCs & expiration codes

SG010118, Exp: 06/2023

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1982-2018
Classification
Class I
Status
Terminated
Recall initiated
Aug 3, 2018
FDA report date
Oct 3, 2018
Quantity
30 100g bags and 12 bottles and 8.4 kg of capsules
Recall type
Voluntary: Firm initiated
Recalling firm
Zakah Life LLC

Original FDA data

Every field from FDA enforcement report F-1982-2018, exactly as published.

Show all FDA fields
City
Ankeny
State
IA
Status
Terminated
Country
United States
Event ID
80729
Address
210 Ne Delaware Ave Ste 240
Code information
SG010118, Exp: 06/2023
Postal code
50021-6714
Report date
Oct 3, 2018
Product type
Food
Recall number
F-1982-2018
Classification
Class I
Recalling firm
Zakah Life LLC
Product quantity
30 100g bags and 12 bottles and 8.4 kg of capsules
Termination date
Oct 26, 2018
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.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
Distributed to consumers and retailers in Colorado, Illinois, Iowa, and Nebraska
Recall initiation date
Aug 3, 2018
Initial firm notification
Telephone
Center classification date
Sep 25, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1982-2018, published Oct 3, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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