CLASS I Food recall · Reported 2 May 2018 · FDA Enforcement Report

Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement recalled by NGB

NGB is recalling Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, distributed nationwide in the US. The recall was initiated on 16 Mar 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
Quantity recalled12,450 Bottles

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-1134-2018
FDA event ID
79794
Recalling firm
NGB, West Jordan, UT
Classification
Class I
Status
Terminated
Recall initiated
16 Mar 2018
FDA classified
25 Apr 2018
Reported
2 May 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Energy Drinks

Timeline

16 Mar 2018Recall initiated by company
25 Apr 2018Classified by FDA+40 days
2 May 2018Published in enforcement report+7 days

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

Reason for recall

NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination.

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

Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules

Where it was distributed

Retailers nationwide. No military/govt/VA/foreign consignees.

Nationwide Virginia

Questions about this recall

Why was it recalled?

NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination.

Which lots are affected?

Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424

Where was it sold?

Retailers nationwide. No military/govt/VA/foreign consignees.

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.

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