CLASS I Food recall · Reported 25 Apr 2018 · FDA Enforcement Report

Nirvanio Maeng Da Kratom all packages, all quantities recalled

Nutrizone is recalling Nirvanio Maeng Da Kratom all packages, all quantities, distributed nationwide in the US. The recall was initiated on 30 Mar 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lots

Quantity recalledApproximately 5517 units

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-1384-2018
FDA event ID: 79672
Recalling firm: Nutrizone, Houston, TX
Brand: Nirvanio Maeng
Classification: Class I
Status: Terminated
Recall initiated: 30 Mar 2018
FDA classified: 7 May 2018
Reported: 25 Apr 2018
Type: Voluntary: Firm initiated
Customers notified by: Press Release
Reason category: Salmonella
Product category: Energy Drinks

Timeline

30 Mar 2018	Recall initiated by company
25 Apr 2018	Published in enforcement report	+26 days
7 May 2018	Classified by FDA	+12 days

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

Reason for recall

Dietary supplements have the potential to be 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

Nirvanio Maeng Da Kratom all packages, all quantities

Where it was distributed

Nationwide (FL, CA,OK,GA,SC,PA,LA,WA,MS,MO,KY,AZ,CO,TX, NY,IL)

Nationwide Arizona California Colorado Florida Georgia Illinois Kentucky Louisiana Missouri Mississippi New York Oklahoma Pennsylvania South Carolina Texas Washington

Questions about this recall

Is Nirvanio Maeng Da Kratom all packages, all quantities recalled?

Yes. Nutrizone recalled Nirvanio Maeng Da Kratom all packages, all quantities on 30 Mar 2018. The recall is Class I and its status is Terminated. Recall number F-1384-2018.

Why was it recalled?

Dietary supplements have the potential to be contaminated with Salmonella.

Which lots are affected?

All lots

Where was it sold?

Nationwide (FL, CA,OK,GA,SC,PA,LA,WA,MS,MO,KY,AZ,CO,TX, NY,IL)

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

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