Sunset Natural Products recalls Prostaliv dietary supplements manufactured since April 2014 due to FDA consent decree requirements. Consumers should stop using products from this lot.
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.
Sunset Natural Products is recalling Prostaliv dietary supplements made since April 2, 2014. This recall follows a consent decree requiring the company to stop marketing supplements until they meet FDA safety standards.
The company is prohibited from marketing dietary supplements until they meet FDA safety standards. This recall is part of a consent decree that requires them to destroy products made since April 2014 and hire a cGMP expert.
Anyone who purchased Prostaliv supplements from Sunset Natural Products since April 2, 2014. People who have used these products are most at risk.
Check for Prostaliv bottles labeled '60 capsules per bottle' with lot number 180215 and expiration date 02/18. Products sold with UPC 897666001144 are affected.
Immediately stop using Prostaliv supplements manufactured since April 2, 2014.
Sunset Natural Products must recall these products as part of a consent decree with the FDA that prohibits them from marketing supplements until they meet safety standards.
Check for Prostaliv bottles with lot number 180215, expiration date 02/18, and UPC 897666001144.
The recall record does not specify a return process, so contact the manufacturer directly for instructions.
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-0541-2016 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0541-2016 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.
