Class IITerminated in FDA datasetOct 5, 2015

Prostaliv, 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.

Check the codes ↓

The exact product

Prostaliv, 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 # 180215 Exp Date 02/18 UPC 897666001144,

TypeCode / valueContext
lot180215Lot # 180215 Exp Date 02/18 UPC 897666001144,

Recall details

Recall number
F-0541-2016
Event ID
72877
FDA status
Terminated
Initiated
Oct 5, 2015
Reported
Feb 24, 2016
Classified
Feb 17, 2016
Terminated
Apr 10, 2017
Quantity
5000 bottles (300,000)
Location
Miami, FL, United States
Initiation type
FDA Mandated
Notification
Other

Where it was distributed

FL and NV

FDA source record · F-0541-2016

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.