The Recall Desk
CriticalFDA (Food)·F-1432-2018·Announced 2018-05-16

Triangle Pharmanaturals Recalls Kratom Products for Salmonella Contamination Risk

Triangle Pharmanaturals LLC is recalling Lifted Kratom Green Maeng Da products due to potential Salmonella contamination.

What this means for you

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The source text explicitly identifies the agency classification as Class I, which mandates a severity score of 5 according to the rubric.

Plain-English summary

Triangle Pharmanaturals LLC is recalling Lifted Kratom Green Maeng Da products, including 45-gram powder, 150-capsule, and 300-capsule plastic bottles. The products were manufactured for Raw Form Organics in Las Vegas, Nevada.

The recall is being conducted because all Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaturals LLC have the potential to be contaminated with Salmonella. The agency has classified this as a Class I recall.

The affected products were distributed in Washington, Georgia, South Carolina, Florida, New Jersey, Louisiana, California, Texas, Nevada, North Carolina, Pennsylvania, Missouri, Colorado, Oregon, Montana, Massachusetts, Utah, Nebraska, Arizona, New York, Ohio, Virginia, and Maryland. Consumers should stop using these products and follow instructions from the recalling firm or the FDA.

The recalled product

Product
Lifted Kratom Green Maeng Da in 45 gram powder, 150 capsule and 300 capsule plastic bottles. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • ALL

Distribution

Part of a larger recall action

This product is one of 26 recalled by TRIANGLE PHARMANATURALS LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 26 products in this recall →