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Molecule Kratom White Maeng Da in 20 capsule, 80 capsule, 45…: FDA Recall F-1422-2018

Agency action: Apr 6, 2018Record ID: F-1422-2018
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What happened

Original notice title

Molecule Kratom White Maeng Da in 20 capsule, 80 capsule, 45 gram powder, and 250 gram powder plastic bottles, recall F-1422-2018

From the archived source record

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

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class I
Recall initiated by
FDA Mandated
Report date
May 16, 2018
Termination date in the archive
Mar 26, 2021
Source checked
Jul 16, 2026
Record revision
81dcfdb59d5c

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

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Source presentation by Dr. Edward M.Kim, PharmD · Clinical Director, SupplementSafety editorial team · How we prepare records

What is affected

Product
Molecule Kratom White Maeng Da in 20 capsule, 80 capsule, 45 gram powder, and 250 gram powder plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Company
TRIANGLE PHARMANATURALS LLC
Lot / identifier
ALL
Market / distribution
WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.