Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
Recalling firm: NGB, Corp
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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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
| Type | Code / value | Context |
|---|---|---|
| lot | 161300 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 161314 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 161323 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 171400 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 171409 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 171424 | 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 171426 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 171473 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 171474 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 181485 | Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 |
| lot | 181487 | Lot: 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.
Data updated September 16, 2026. View official FDA data ↗
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