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
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
- Brand
- Nxtgen Botanicals
- 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 2018 | Recall initiated by company | |
| 25 Apr 2018 | Classified by FDA | +40 days |
| 2 May 2018 | Published 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.
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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