FDA recall record
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
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 August 17, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Reason
Multiple products marketed as dietary supplements are unapproved new drugs based on disease claims or routes of administration.
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.
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Code information listed by FDA
50070340, 55837004
Distribution and firm information
Recalling firm listed by FDA: Grato Holdings, Inc.
Firm location listed by FDA: Woodbine, IA, United States
Distribution reported by FDA: Shipped to customers nationwide and Canada.
Product quantity listed by FDA: 767 120-tablet 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.