FDA recall record
Prostamax DUO, 60 capsules per bottle. Manufactured by Sunset Natural Products
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
Prostamax DUO, 60 capsules per bottle. Manufactured by Sunset Natural Products
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 manufatured 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.
Prostamax DUO, 60 capsules per bottle. Manufactured by Sunset Natural Products
Code information listed by FDA
Lot # 140515 Exp. Date 05/18 UPC 850993004055,
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: FL and NV
Product quantity listed by FDA: 4,000 bottles (240,000 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.