FDA recall record
Dragon Maeng Da Kratom Powder: 60 g and 150 g bottle. Dragon Maeng Da Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 6, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Dragon Maeng Da Kratom Powder: 60 g and 150 g bottle. Dragon Maeng Da Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles.
Reason
Samples collected by public health officials found the presence of Salmonella.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Dragon Maeng Da Kratom Powder: 60 g and 150 g bottle. Dragon Maeng Da Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles.
Code information listed by FDA
unknown
Distribution and firm information
Recalling firm listed by FDA: Maya Distribution, LLC
Firm location listed by FDA: Salt Lake City, UT, United States
Distribution reported by FDA: Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.
Product quantity listed by FDA: unknown
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.