FDA recall record
Dragon Malaysian Kratom Powder: 150 g bottle. Dragon Malaysian Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles. Dragon Malaysian Kratom: 20-ct x 500 mg capsules in pouc...
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 Malaysian Kratom Powder: 150 g bottle. Dragon Malaysian Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles. Dragon Malaysian Kratom: 20-ct x 500 mg capsules in pouches.
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 Malaysian Kratom Powder: 150 g bottle. Dragon Malaysian Kratom: 200-, 80-, and 40-ct x 500mg capsules in bottles. Dragon Malaysian Kratom: 20-ct x 500 mg capsules in pouches.
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.