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Class I: serious health riskTerminated

Triangle Pharmanaturals Molecule Kratom White Borneo in 20 capsule Recall

Molecule Kratom White Borneo in 20 capsule, 80 capsule, 45 gram powder, and 250 gram po…

TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

Risk level
Class I
Reported by FDA
May 16, 2018
Recall ID
F-1423-2018
Check your lot numberHow we source this data

Summary

Triangle Pharmanaturals recalled Molecule Kratom White Borneo in 20 capsule starting Apr 6, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-1423-2018 on May 16, 2018. Reason: All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella. Status: Terminated.

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

Product description

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

Lot numbers, UPCs & expiration codes

ALL

Where it was 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 to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1423-2018
Classification
Class I
Status
Terminated
Recall initiated
Apr 6, 2018
FDA report date
May 16, 2018
Quantity
N/A
Recall type
FDA Mandated
Recalling firm
TRIANGLE PHARMANATURALS LLC

Original FDA data

Every field from FDA enforcement report F-1423-2018, exactly as published.

Show all FDA fields
City
Las Vegas
State
NV
Status
Terminated
Country
United States
Event ID
79806
Address
5320 Cameron St Ste 7
Code information
ALL
Postal code
89118-2234
Report date
May 16, 2018
Product type
Food
Recall number
F-1423-2018
Classification
Class I
Recalling firm
TRIANGLE PHARMANATURALS LLC
Termination date
Mar 26, 2021
Reason for recall
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Voluntary / mandated
FDA Mandated
Product description
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
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.
Recall initiation date
Apr 6, 2018
Initial firm notification
Letter
Center classification date
May 10, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1423-2018, published May 16, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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