Argindione, sold as bulk of 50,000 capsules.
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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FDA code information
Lot # 480514 Exp. Date 05/17 and Lot # 320614 Exp. Date 06/17
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Full FDA record and distribution details
Original product description
Argindione, sold as bulk of 50,000 capsules.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | 320614 | Lot # 480514 Exp. Date 05/17 and Lot # 320614 Exp. Date 06/17 |
| lot | 480514 | Lot # 480514 Exp. Date 05/17 and Lot # 320614 Exp. Date 06/17 |
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-0537-2016
- Event ID
- 72877
- FDA status
- Terminated
- Initiated
- Oct 5, 2015
- Reported
- Feb 24, 2016
- Classified
- Feb 17, 2016
- Terminated
- Apr 10, 2017
- Quantity
- 100,000 capsules
- 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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