Eden's Ethnos Kratom Powder Recalled Due to Salmonella Contamination
Eden's Ethnos LLC is recalling 2,775 kilograms of bulk Kratom powder because FDA and state samples found Salmonella. The product was distributed in five states.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The recall is classified as FDA Class I, which meets the rubric criteria for a Critical severity score.
Plain-English summary
Eden's Ethnos, LLC is recalling 2,775 kilograms of Eden's Ethnos Bulk Kratom powder, sold in 25-kilogram bags. The product is also known by several names, including K. Bali Supreme, K Maeng Da Supreme, K Green Vein, Green Maeng Da, K Red Maeng Da, K Red Bali, and K Green Bali. The recall was initiated after FDA and state samples found Salmonella in Kratom products that traced back to the company.
The recalled product was distributed in Florida, Missouri, Oregon, California, and Utah. No specific lot codes are associated with this recall. Consumers who purchased this product should stop using it and contact the distributor for further instructions.
The recalled product
- Product
- 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
- Manufacturer
- Eden's Ethnos, LLC
- Category
- Food — Herbal Supplements
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- No Codes
Distribution
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