Drug & medication recalls High risk

Maeng Da 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 Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 1…
Recall number
D-0989-2019
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

Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.

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