CLASS I Food recall · Reported 16 May 2018 · FDA Enforcement Report

Third Eye Kratom White recalled by Triangle Pharmanaturals

Triangle Pharmanaturals is recalling Third Eye Kratom White, distributed in 23 states. The recall was initiated on 6 Apr 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesALL

Quantity recalledN/A

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-1436-2018
FDA event ID: 79806
Recalling firm: Triangle Pharmanaturals, Las Vegas, NV
Brand: Third Eye
Classification: Class I
Status: Terminated
Recall initiated: 6 Apr 2018
FDA classified: 10 May 2018
Reported: 16 May 2018
Type: FDA Mandated
Customers notified by: Letter
Reason category: Salmonella
Product category: Energy Drinks

Timeline

6 Apr 2018	Recall initiated by company
10 May 2018	Classified by FDA	+34 days
16 May 2018	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Third Eye Kratom White in 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119

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.

Arizona California Colorado Florida Georgia Louisiana Massachusetts Maryland Missouri Montana North Carolina Nebraska New Jersey Nevada New York Ohio Oregon Pennsylvania South Carolina Texas

Questions about this recall

Is Third Eye Kratom White recalled?

Yes. Triangle Pharmanaturals recalled Third Eye Kratom White on 6 Apr 2018. The recall is Class I and its status is Terminated. Recall number F-1436-2018.

Why was it recalled?

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

Which lots are affected?

ALL

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Triangle Pharmanaturals

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Reported	Class	Recall	Company	Reason	Where
16 May 2018Food	CLASS I	Raw Form Organics Maeng Da Kratom Amethyst Gold recalled	Triangle Pharmanaturals	Salmonella	23 states
16 May 2018Food	CLASS I	Molecule Kratom White Borneo in powder, and powder recalledMolecule Kratom	Triangle Pharmanaturals	Salmonella	23 states
16 May 2018Food	CLASS I	Live Well Kratom Green Maeng Da recalled by Triangle PharmanaturalsLive Well	Triangle Pharmanaturals	Salmonella	23 states
16 May 2018Food	CLASS I	Raw Form Organics Maeng Da Kratom Emerald Green recalled	Triangle Pharmanaturals	Salmonella	23 states
16 May 2018Food	CLASS I	Molecule Kratom Red Malay recalled by Triangle PharmanaturalsMolecule Kratom	Triangle Pharmanaturals	Salmonella	23 states

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