White Vein Kratom — Class I drug recall D-0988-2019
Terminated recall by Todd Holiday dba Sunstone Organics, reported 2019-03-13, distributed in CA, NE, OR, WA. MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
| Recall number | D-0988-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Todd Holiday dba Sunstone Organics, Springfield, OR, United States |
| Recall initiated | 2019-02-13 |
| Classified | 2019-03-11 |
| Reported by FDA | 2019-03-13 |
| Terminated | 2023-02-14 |
| Distributed | CA, NE, OR, WA |
| Reason classes | microbial contamination, sterility |
| Pathogens | salmonella |
| UPC / GTIN / UDI-DI | 00859667007347, 00859667007354, 00859667007361 |
| Lot numbers | 119 |
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 for recall
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0988-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.