FDA recall record
Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
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
Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
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.
Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
Code information listed by FDA
A107911115, A110400216, X016652L1
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: 65,195 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.