Moinsage, 60 capsules per bottle.
Recalling firm: Sunset Natural Products Inc.
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.
The exact product
Moinsage, 60 capsules per bottle. Manufactured by Sunset Natural Products
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot # 030615 Exp. Date 07/18 UPC 897666001164
| Type | Code / value | Context |
|---|---|---|
| UPC | 897666001164 | Lot # 030615 Exp. Date 07/18 UPC 897666001164 |
| lot | 030615 | Lot # 030615 Exp. Date 07/18 UPC 897666001164 |
Recall details
- Recall number
- F-0539-2016
- Event ID
- 72877
- FDA status
- Terminated
- Initiated
- Oct 5, 2015
- Reported
- Feb 24, 2016
- Classified
- Feb 17, 2016
- Terminated
- Apr 10, 2017
- Quantity
- 5,000 bottles (300,000 caps)
- Location
- Miami, FL, United States
- Initiation type
- FDA Mandated
- Notification
- Other
Where it was distributed
FL and NV
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.