Triangle Pharmanaturals Recalls Kratom Products Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling Molecule Kratom White Borneo products in various formats 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 agency classified this as an FDA Class I recall, which mandates a severity score of 5 according to the rubric.
Plain-English summary
Triangle Pharmanaturals LLC is recalling Molecule Kratom White Borneo products, including 20 and 80 capsule bottles, as well as 45 and 250 gram powder bottles. The products were manufactured for Raw Form Organics in Las Vegas, Nevada.
The recall was issued 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 contact the recalling firm for instructions on disposal or return.
The recalled product
- Product
- 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
- Manufacturer
- TRIANGLE PHARMANATURALS LLC
- Category
- Food — Supplements
- Hazard
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 →Related recalls
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