FDA Drug recall D-0989-2019
Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (U…
- FDA Drug
- Class I
- terminated
- Published 2019-03-13
On 2019-03-13 the FDA classified a Class I recall of Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (U… by Todd Holiday, citing MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0989-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2019-02-13 |
| Published | 2019-03-13 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Todd Holiday |
| Distribution | CA, NE, OR, WA |
Product
Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
Reason
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Identifiers
| upc | 00859667007149 |
|---|---|
| upc | 00859667007156 |
| upc | 00859667007163 |
| code_info | Lot #124A |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0989-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.