Eden's Eth: Bulk Kratom Powder Recall - Salmonella Risk
Eden's Ethnos LLC recalls bulk kratom powder products due to Salmonella contamination found in FDA and state samples. Consumers should avoid using these products.
Lower-risk recall
FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.
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What happened, in plain English
Eden's Ethnos LLC is recalling bulk kratom powder products that were found to contain Salmonella by the FDA and state health authorities. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/19198-eden-s-eth-bulk-kratom-powder-recall-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19198-eden-s-eth-bulk-kratom-powder-recall-salmonella-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-1439-2018
Cite this page
“Eden's Eth: Bulk Kratom Powder Recall - Salmonella Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19198-eden-s-eth-bulk-kratom-powder-recall-salmonella-risk. Based on FDA recall #F-1439-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1439-2018%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and stomach cramps. The contamination was detected in FDA and state samples from Eden's Ethnos products.
Who’s affected
Anyone who purchased Eden's Ethnos bulk kratom powder products, including those labeled as K. Bali Supreme, K Maeng Da Supreme, etc. The risk is low for most users as Salmonella is typically not life-threatening in small amounts.
How to tell if you have this one
Check for Eden's Ethnos bulk kratom powder products in kilogram bags, including those labeled as K. Bali Supreme, K Maeng Da Supreme, K Green Vein, Green, or other similar names. These products were distributed by Eden's Ethnos LLC in Carlsbad, CA.
- Brand
Eden's Ethnos- Category
Food
What to do — step by step
Check Product Labels
Look for Eden's Ethnos bulk kratom powder products in kilogram bags with labels such as K. Bali Supreme, K Maeng Da Supreme, K Green Vein, or Green.
Where it went and when
Where it was distributed
Distributed in 5 states.
FDA distribution: “FL, MO, OR, CA, UT” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Missouri, Oregon, Utah.
Recall timeline
FDA terminated this recall 2 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-1439-2018 (April 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1439-2018 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.