FDA recall record

Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also called K recall — FDA F-1439-2018

FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.

Class Iclassification
F-1439-2018official record ID
May 16, 2018report date

Recall record at a glance

Official recordF-1439-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmEden's Ethnos, LLC
Report dateMay 16, 2018
Recall initiation dateApr 20, 2018
Quantity2,775 kilograms
LocationCarlsbad, CA, United States

Official product description

Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also called K. Bali Supreme, K Maeng Da Supreme, K Green Vein, Green Maeng Da, K Red Maeng Da, K Red Bali, K Green Bali Distributed by Eden Ethnos LLC, Carlsbad, CA 92010

Why the product was recalled

FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.

Distribution information

FL, MO, OR, CA, UT

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.