Class ITerminated in FDA datasetRecall initiated Apr 6, 2018

Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles;…

Recalling firm: TRIANGLE PHARMANATURALS LLC

Why it was recalled

All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 26, 2021.

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ProductRaw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119

FDA code information

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Full FDA record and distribution details

Original product description

Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119

Original FDA recall reason

All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

Recall details

Recall number
F-1413-2018
Event ID
79806
FDA status
Terminated
Initiated
Apr 6, 2018
Reported
May 16, 2018
Classified
May 10, 2018
Terminated
Mar 26, 2021
Quantity
N/A
Location
Las Vegas, NV, United States
Initiation type
FDA Mandated
Notification
Letter

Where it was distributed

WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

FDA source record · F-1413-2018

Data updated September 16, 2026. View official FDA data ↗

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