F-0539-2016 Class II Terminated
FDA food recall F-0539-2016 was initiated by Sunset Natural Products Inc. on Oct 5, 2015 and is designated Class II. Reason for recall: 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… The recall status is terminated (terminated Apr 10, 2017). Affected quantity: 5,000 bottles (300,000 caps).
Recall Details
- Product Type
- Food
- Report Date
- Feb 24, 2016
- Initiation Date
- Oct 5, 2015
- Termination Date
- Apr 10, 2017
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 5,000 bottles (300,000 caps)
Product Description
Moinsage, 60 capsules per bottle. Manufactured by Sunset Natural Products
Reason for Recall
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.
Distribution Pattern
FL and NV
Code Information
Lot # 030615 Exp. Date 07/18 UPC 897666001164
Source
- Dataset
- openFDA food recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for F-0539-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 23, 2026