FDA recall record
Chardon De Marie, 60 capsules per bottle
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 April 10, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Chardon De Marie, 60 capsules per bottle
Reason
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
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.
Chardon De Marie, 60 capsules per bottle
Code information listed by FDA
" The Decree was entered on September 25, 2015. Known lots and expiration dates: Lot # 290414 Exp. Date 04/17, Lot # 280414 Exp. Date 05/17, Lot # 660514 Exp. Date 06/17, Lot # 030714 Exp. Date 07/17, Lot # 670514 Exp. Date 07/17, Lot # 680514 Exp. Date 10/17, Lot # 131214 Exp. Date 12/17, Lot # 151214 Exp. Date 02/18
Distribution and firm information
Recalling firm listed by FDA: Sunset Natural Products Inc.
Firm location listed by FDA: Miami, FL, United States
Distribution reported by FDA: Products distributed to Florida, Nevada and the Dominican Republic
Product quantity listed by FDA: 23,665 Bottles, (1,420,000 capsules)
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.