Tamarack Eclipse Kratom Products Recall: Salmonella Contamination Risk
Tamarack Inc. recalls Eclipse Kratom Premium Maeng Da capsules and bottles due to potential Salmonella contamination. Consumers should stop using these products immediately.
Stop using this now
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
Contact the company
What happened, in plain English
Tamarack Inc. is recalling Eclipse Kratom Premium Maeng Da products because they may be contaminated with Salmonella. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/19531-tamarack-eclipse-kratom-products-recall-salmonella-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19531-tamarack-eclipse-kratom-products-recall-salmonella-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0992-2018
Cite this page
“Tamarack Eclipse Kratom Products Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19531-tamarack-eclipse-kratom-products-recall-salmonella-contamination-risk. Based on FDA recall #F-0992-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0992-2018%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning. If present in Kratom products, it may lead to symptoms like diarrhea, fever, and abdominal cramps if ingested.
Who’s affected
Anyone who owns or uses Eclipse Kratom Premium Maeng Da capsules or 2 oz bottles. People with weakened immune systems are at higher risk of serious illness.
How to tell if you have this one
Check for Eclipse Kratom Premium Maeng Da products with 40 count capsules or 2 oz bottles. These products were distributed by Tamarack Inc. in Cheyenne, WY and are available on the market.
- Brand
Tamarack- Category
Food
What to do — step by step
Stop Using Products
Immediately stop using Eclipse Kratom Premium Maeng Da capsules or 2 oz bottles if you have them.
Where it went and when
Where it was distributed
Distributed in Utah.
FDA distribution: “Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Utah.
Recall timeline
FDA terminated this recall 2 years 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-0992-2018 (March 19, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0992-2018 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.