Class ITerminated in FDA datasetRecall initiated Mar 16, 2018

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

Recalling firm: NGB, Corp

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 22, 2020.

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

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
lot161300Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot161314Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot161323Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot171400Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot171409Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot171424171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot171426Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot171473Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot171474Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot181485Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
lot181487Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424

Original FDA recall reason

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

Recall details

Recall number
F-1134-2018
Event ID
79794
FDA status
Terminated
Initiated
Mar 16, 2018
Reported
May 2, 2018
Classified
Apr 25, 2018
Terminated
Jan 22, 2020
Quantity
12,450 Bottles
Location
West Jordan, UT, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

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

FDA source record · F-1134-2018

Data updated September 16, 2026. View official FDA data ↗

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