NGB Corp Recalls Maeng Da Kratom Supplements Due to Salmonella Risk
NGB Corp is recalling Maeng Da Kratom dietary supplements after potential Salmonella contamination in specific lots. Consumers should check product labels for affected lots and contact the company for guidance.
Use caution until it’s fixed
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Contact the company
What happened, in plain English
NGB Corp is recalling Maeng Da Kratom dietary supplements that may contain Salmonella. This poses a risk of foodborne illness if consumed, so affected consumers should stop using the product. Read more at govinfonow.com/recall/19541-ngb-corp-recalls-maeng-da-kratom-supplements-due-to-salmonella.
Source Summary by GovInfoNow · govinfonow.com/recall/19541-ngb-corp-recalls-maeng-da-kratom-supplements-due-to-salmonella · Updated October 7, 2026 · FDA enforcement record: FDA #F-1134-2018
Cite this page
“NGB Corp Recalls Maeng Da Kratom Supplements Due to Salmonella Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19541-ngb-corp-recalls-maeng-da-kratom-supplements-due-to-salmonella. Based on FDA recall #F-1134-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1134-2018%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. Consuming contaminated supplements may result in these health issues, especially for those with compromised immune systems.
Who’s affected
Anyone who purchased the recalled Maeng Da Kratom supplements between the listed production dates. People with weakened immune systems are at higher risk for foodborne illness.
How to tell if you have this one
Check the product label for the lot numbers: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424. The product is a dietary supplement containing Maeng Da Kratom.
- Brand
NGB Corp- Category
Food
What to do — step by step
Check Product Lot Number
Look for the lot numbers listed: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424 on the product label.
Stop Using Product
If your product has a listed lot number, stop using it immediately to avoid potential Salmonella contamination.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Retailers nationwide. No military/govt/VA/foreign consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1134-2018 (March 16, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1134-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.