Recalls / Class I
Class IF-1434-2018
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Live Well Kratom Green Maeng Da in 150 capsule and 300 capsule plastic bottles. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
- Type
- Food
- Affected lot / code info
- ALL
- Quantity
- N/A
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
Recalling firm
- Firm
- TRIANGLE PHARMANATURALS LLC
- Notification channel
- Letter
- Type
- FDA Mandated
- Address
- 5320 Cameron St Ste 7, N/A, Las Vegas, Nevada 89118-2234
Distribution
- 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.
Timeline
- Recall initiated
- 2018-04-06
- FDA classified
- 2018-05-10
- Posted by FDA
- 2018-05-16
- Terminated
- 2021-03-26
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1434-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings.