FDA recall D-0988-2019

Todd Holiday dba Sunstone Organics · Class I · drug

Product

White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules (UPC 00859667007361), Sunstone Organics Springfield, Oregon 97473 541-972-3327.

Reason for recall

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.

Distribution

California, Nebraska, Oregon, Washington

Key facts

Status: Terminated
Initiation date: 2019-02-13
Report date: 2019-03-13
Termination date: 2023-02-14
Voluntary/Mandated: Voluntary: Firm initiated
Location: Springfield, OR, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0988-2019