Moinsage, 60 capsules per bottle.
Recalling firm: Sunset Natural Products Inc.
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 10, 2017.
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897666001164FDA code information
Lot # 030615 Exp. Date 07/18 UPC 897666001164
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Full FDA record and distribution details
Original product description
Moinsage, 60 capsules per bottle. Manufactured by Sunset Natural Products
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 897666001164 | Lot # 030615 Exp. Date 07/18 UPC 897666001164 |
| lot | 030615 | Lot # 030615 Exp. Date 07/18 UPC 897666001164 |
Original FDA recall 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.
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 ↗
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