Lifted Kratom Green Maeng Da in 45 gram powder, 150 capsule and 300 capsule plastic bottles.…
Recalling firm: TRIANGLE PHARMANATURALS LLC
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 26, 2021.
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FDA code information
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Full FDA record and distribution details
Original product description
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
Original FDA recall reason
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
Recall details
- Recall number
- F-1432-2018
- Event ID
- 79806
- FDA status
- Terminated
- Initiated
- Apr 6, 2018
- Reported
- May 16, 2018
- Classified
- May 10, 2018
- Terminated
- Mar 26, 2021
- Quantity
- N/A
- Location
- Las Vegas, NV, United States
- Initiation type
- FDA Mandated
- Notification
- Letter
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.
Data updated September 16, 2026. View official FDA data ↗
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