Sunset Natural Products recalls Prostaliv New dietary supplements manufactured from April 2, 2014. These products must be destroyed under FDA supervision due to a consent decree.
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.
Sunset Natural Products is recalling Prostaliv New dietary supplements made from April 2, 2014. The recall is required by a court order because the company failed to follow FDA regulations and must destroy all affected products.
The company violated FDA regulations by marketing dietary supplements without proper oversight. This led to a court-ordered recall to ensure compliance with food safety laws.
Owners of Prostaliv New supplements purchased between April 2, 2014, and September 25, 2015. People who have these products are at risk of legal consequences if they do not destroy them.
Check for Prostaliv New supplements with lot numbers 400514, 180614, 190614, or 650614, all expiring by June 17 or August 17, 2017.
Sunset Natural Products requires all recalled Prostaliv New supplements to be destroyed under FDA supervision.
The company violated FDA regulations and must destroy all products made from April 2, 2014, to comply with a court order.
Prostaliv New supplements with lot numbers 400514, 180614, 190614, or 650614, expiring by June 17 or August 17, 2017.
Check the lot number on the product label; affected lots are 400514, 180614, 190614, or 650614, all expiring by June 17 or August 17, 2017.
We’ve drafted a message you can send Sunset Natural Products to request your refund or repair — edit it as you like.
Subject: Recall F-0961-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0961-2017 from Sunset Natural Products. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
