Prostaliv, 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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FDA code information
As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with the procedures provided in paragraph 6, ALL dietary supplements that were manufactured, prepared, processed, packed, labeled, held and/or distributed between April 2, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lots and expiration dates: Lot # 390514 Exp. Date 06/17, Lot # 350614 Exp. Date 06/17, Lot # 630614 Exp. Date 06/17, Lot # 640614 Exp. Date 06/17, Lot # 670614 Exp. Date 08/17, Lot # 421014 Exp. Date 11/17, Lot # 431014 Exp. Date 12/17
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Full FDA record and distribution details
Original product description
Prostaliv, 60 capsules per bottle
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | 350614 | , 2015. Known lots and expiration dates: Lot # 390514 Exp. Date 06/17, Lot # 350614 Exp. Date 06/17, Lot # 630614 Exp. Date 06/17, Lot # 640614 Exp. Date 06/17, Lot # 670614 Exp. Date 08/17, Lot # 4210 |
| lot | 390514 | ee was entered on September 25, 2015. Known lots and expiration dates: Lot # 390514 Exp. Date 06/17, Lot # 350614 Exp. Date 06/17, Lot # 630614 Exp. Date 06/17, Lot # 640614 Exp. Date 06/17, Lot # 6706 |
| lot | 421014 | Date 06/17, Lot # 640614 Exp. Date 06/17, Lot # 670614 Exp. Date 08/17, Lot # 421014 Exp. Date 11/17, Lot # 431014 Exp. Date 12/17 |
| lot | 431014 | Date 06/17, Lot # 670614 Exp. Date 08/17, Lot # 421014 Exp. Date 11/17, Lot # 431014 Exp. Date 12/17 |
| lot | 630614 | ation dates: Lot # 390514 Exp. Date 06/17, Lot # 350614 Exp. Date 06/17, Lot # 630614 Exp. Date 06/17, Lot # 640614 Exp. Date 06/17, Lot # 670614 Exp. Date 08/17, Lot # 421014 Exp. Date 11/17, Lot # 4310 |
| lot | 640614 | Date 06/17, Lot # 350614 Exp. Date 06/17, Lot # 630614 Exp. Date 06/17, Lot # 640614 Exp. Date 06/17, Lot # 670614 Exp. Date 08/17, Lot # 421014 Exp. Date 11/17, Lot # 431014 Exp. Date 12/17 |
| lot | 670614 | Date 06/17, Lot # 630614 Exp. Date 06/17, Lot # 640614 Exp. Date 06/17, Lot # 670614 Exp. Date 08/17, Lot # 421014 Exp. Date 11/17, Lot # 431014 Exp. Date 12/17 |
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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Recall details
- Recall number
- F-0960-2017
- Event ID
- 74054
- FDA status
- Terminated
- Initiated
- Oct 13, 2015
- Reported
- Jan 4, 2017
- Classified
- Dec 28, 2016
- Terminated
- Apr 10, 2017
- Quantity
- 20,499 Bottles, (1,500,000 capsules)
- Location
- Miami, FL, United States
- Initiation type
- FDA Mandated
- Notification
- Letter
Where it was distributed
Products distributed to Florida, Nevada and the Dominican Republic
Data updated September 16, 2026. View official FDA data ↗
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