Eden's Ethnos, LLC Recall: FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.
United States
TerminatedClass I
- Company
- Eden's Ethnos, LLC
- Product
- Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also call…
- Recall date
- April 20, 2018
- Terminated
- June 25, 2018
- Source
- FDA
Reason for recall
FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 2,775 kilograms | No Codes |
Distribution
- FL
- MO
- OR
- CA
- UT
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1439-2018
- Event ID
- 79951
- Status
- Terminated
- Classification
- Class I
- Company
- Eden's Ethnos, LLC
- 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
- Quantity
- 2,775 kilograms
- Reason
- FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.
- Recall initiation date
- April 20, 2018
- Report date
- May 16, 2018
- Classification date
- Not published in this source record
- Termination date
- June 25, 2018
- Distribution pattern
- FL, MO, OR, CA, UT
- UPC, lot, and code information
- No Codes
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Eden's Ethnos, LLC
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Florida | 1 |
| Missouri | 1 |
| Oregon | 1 |
| California | 1 |
| Utah | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
