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

Triangle Pharmanaturals LLC recalled Lifted Kratom Green Maeng Da in 45 gram powder, 150 capsule and 300 capsule plastic bottles. in a Class I action — the FDA's most serious tier, reserved for products with a reasonable probability of causing serious health consequences or death on Apr 6, 2018.

The recall was triggered by possible Salmonella contamination: "All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella" Salmonella is one of the most common causes of U.S. foodborne illness, with symptoms that typically appear within six hours to six days of exposure.

The product reached multiple states, recorded by the FDA as "WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Las Vegas, NV. The recall covers N/A of product. The FDA has Terminated this recall (first reported May 16, 2018), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.