Home / Recalls / TRIANGLE PHARMANATURALS LLC / F-1425-2018

F-1425-2018 Class I Terminated

Recalled by TRIANGLE PHARMANATURALS LLC — Las Vegas, NV

FDA food recall F-1425-2018 was initiated by TRIANGLE PHARMANATURALS LLC on Apr 6, 2018 and is designated Class I. Reason for recall: All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella The recall status is terminated (terminated Mar 26, 2021). Affected quantity: N/A.

Recall Details

Product Type: Food
Report Date: May 16, 2018
Initiation Date: Apr 6, 2018
Termination Date: Mar 26, 2021
Voluntary/Mandated: FDA Mandated
Product Quantity: N/A

Product Description

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

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 Pattern

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

Code Information

ALL

Source

Dataset: openFDA food recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for F-1425-2018
openFDA file date: Oct 6, 2026
Loaded by RegDataLab: Oct 6, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.

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