Aval: NXTGEN Kratom Capsules Recall for Salmonella Risk
Avalon Packaging recalls 70-capsule Kratom supplements due to potential Salmonella contamination. Consumers should check lot numbers for affected products.
Lower-risk recall
Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.
Contact the company
What happened, in plain English
Avalon Packaging is recalling NXTGEN Botanicals Kratom supplements because they may contain Salmonella. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/19584-aval-nxtgen-kratom-capsules-recall-for-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19584-aval-nxtgen-kratom-capsules-recall-for-salmonella-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0996-2018
Cite this page
“Aval: NXTGEN Kratom Capsules Recall for Salmonella Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19584-aval-nxtgen-kratom-capsules-recall-for-salmonella-risk. Based on FDA recall #F-0996-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0996-2018%22&limit=1).
Why it’s dangerous
Salmonella is a bacterium that can cause food poisoning. If the Kratom supplements are contaminated, eating them could lead to symptoms like diarrhea, fever, and stomach cramps.
Who’s affected
Anyone who purchased the 70-capsule Kratom supplements made in the U.S.A. Lot 171409. People with compromised immune systems are at higher risk.
How to tell if you have this one
Check for the product name 'NXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules' and lot number 171409. Products were made in the U.S.A.
- Brand
Avalon Packaging- Category
Food
What to do — step by step
Check Product Details
Look for the lot number 171409 on the product label to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in Utah.
FDA distribution: “Sold to Label owner in UT.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Utah.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product safe to use?
The recall states there is a potential for Salmonella contamination, so it is not recommended to consume the affected product.
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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-0996-2018 (March 9, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0996-2018 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.