FDA recall record
Devagrass
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 20, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Devagrass
Reason
West Coast Laboratories is recalling Xambo and Devagrass because there may be presence of 1,3-dimethylamylamine (DMAA).
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.
Devagrass
Code information listed by FDA
Lot No. CK15005 Mfg. Lot no. 620815
Distribution and firm information
Recalling firm listed by FDA: West Coast Laboratories Inc
Firm location listed by FDA: Gardena, CA, United States
Distribution reported by FDA: Colombia, South America
Product quantity listed by FDA: 3,600 blisters
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.