FDA recall record
Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
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 January 22, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
Reason
NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination.
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.
Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
Code information listed by FDA
Lot: 171426, 171473, 161323, 161314, 171409, 171400, 161300, 171474, 181485, 181487, 171424
Distribution and firm information
Recalling firm listed by FDA: NGB, Corp
Firm location listed by FDA: West Jordan, UT, United States
Distribution reported by FDA: Retailers nationwide. No military/govt/VA/foreign consignees.
Product quantity listed by FDA: 12,450 Bottles
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.