Recalls / Class II
Class IIF-0539-2016
Product
Moinsage, 60 capsules per bottle. Manufactured by Sunset Natural Products
- Type
- Food
- Affected lot / code info
- Lot # 030615 Exp. Date 07/18 UPC 897666001164
- Quantity
- 5,000 bottles (300,000 caps)
Why it was recalled
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.
Recalling firm
- Firm
- Sunset Natural Products Inc.
- Notification channel
- Other
- Type
- FDA Mandated
- Address
- 7345 SW 45th St, Miami, Florida 33155-4509
Distribution
- Distribution pattern
- FL and NV
Timeline
- Recall initiated
- 2015-10-05
- FDA classified
- 2016-02-17
- Posted by FDA
- 2016-02-24
- Terminated
- 2017-04-10
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0539-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings.