FDA Drug recall D-0988-2019
White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules…
- FDA Drug
- Class I
- terminated
- Published 2019-03-13
On 2019-03-13 the FDA classified a Class I recall of White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules… 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-0988-2019 |
| 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
White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules (UPC 00859667007361), Sunstone Organics Springfield, Oregon 97473 541-972-3327.
Reason
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Identifiers
| upc | 00859667007347 |
|---|---|
| upc | 00859667007354 |
| upc | 00859667007361 |
| code_info | Lot #119 |
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-0988-2019%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.