Live Well Kratom Green Maeng Da in 150 capsule and 300 capsule… — Class I food recall F-1434-2018
Terminated recall by TRIANGLE PHARMANATURALS LLC, reported 2018-05-16, distributed in AZ, CA, CO, FL, GA, LA, MA, MD…. All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the pote
| Recall number | F-1434-2018 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | TRIANGLE PHARMANATURALS LLC, Las Vegas, NV, United States |
| Recall initiated | 2018-04-06 |
| Classified | 2018-05-10 |
| Reported by FDA | 2018-05-16 |
| Terminated | 2021-03-26 |
| Distributed | AZ, CA, CO, FL, GA, LA, MA, MD, MO, MT, NC, NE, NJ, NV, NY, OH, OR, PA, SC, TX, UT, VA, WA |
| Reason classes | microbial contamination |
| Pathogens | salmonella |
Product
Live Well Kratom Green Maeng Da in 150 capsule and 300 capsule plastic bottles. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Reason for recall
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with 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/F-1434-2018. 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.