White Vein Kratom recalled over Salmonella risk

Recall date

February 13, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Todd Holiday dba Sunstone Organics recalls White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c)…

Recall number

D-0988-2019

FDA classification

Class I

Brand / firm

Todd Holiday dba Sunstone Organics

Sold / distributed

California, Nebraska, Oregon, Washington

Why it was recalled

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

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

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.