FDA recall record
DNPX Powder, 30 Green Apple
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 February 6, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
DNPX Powder, 30 Green Apple
Reason
Product contains the unapproved ingredient, picamilon.
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.
DNPX Powder, 30 Green Apple
Code information listed by FDA
A106770915
Distribution and firm information
Recalling firm listed by FDA: ProSupps USA LLC
Firm location listed by FDA: Plano, TX, United States
Distribution reported by FDA: US and Canada
Product quantity listed by FDA: 694 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.