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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