FDA recall record
Club 13 Kratom Maeng Da Red XS capsules; 5, 20, 25, 40, 50 capsule 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 March 25, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Club 13 Kratom Maeng Da Red XS capsules; 5, 20, 25, 40, 50 capsule bottles
Reason
Samples of Maeng Da red powder were tested and resulted positive for 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.
Club 13 Kratom Maeng Da Red XS capsules; 5, 20, 25, 40, 50 capsule bottles
Code information listed by FDA
Lots # KRXS020718, KRXS030618, KRXS102417, KRXS110617, and KRXS120117.
Distribution and firm information
Recalling firm listed by FDA: Club 13 Enterprises Warehouse
Firm location listed by FDA: Saint Augustine, FL, United States
Distribution reported by FDA: U.S. consignees only.
Product quantity listed by FDA: 873 units
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.