Chameleon Kratom Formula 51 in 60 capsule plastic bottles recalled over Salmonella risk

Recall date

April 6, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

TRIANGLE PHARMANATURALS LLC recalls Chameleon Kratom Formula 51 in 60 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by T…

Recall number

F-1425-2018

FDA classification

Class I

Brand / firm

TRIANGLE PHARMANATURALS LLC

Sold / 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.

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

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Chameleon Kratom Formula 51 in 60 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119