PlainRecalls
FDA Drug Critical Class I Terminated

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.

Reported: March 13, 2019 Initiated: February 13, 2019 #D-0988-2019

Product Description

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.

Details

Units Affected
N/A
Distribution
California, Nebraska, Oregon, Washington
Location
Springfield, OR

Frequently Asked Questions

What product 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.. Recalled by Todd Holiday dba Sunstone Organics. Units affected: N/A.
Why was this product recalled?
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 13, 2019. Severity: Critical. Recall number: D-0988-2019.