Recalls / Class I
Class IF-1424-2018
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
Chameleon Kratom Formula 27 in 60 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-1424-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings.