FDA recall F-1423-2018

Product

Molecule Kratom White Borneo 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

Reason for recall

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

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.

Key facts

Status

Terminated

Initiation date

2018-04-06

Report date

2018-05-16

Termination date

2021-03-26

Voluntary/Mandated

FDA Mandated

Location

Las Vegas, NV, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1423-2018