Sunset Natural Products recalls 250,000 Artrosamin capsules made from April 2, 2014, due to a consent decree requiring destruction under FDA supervision.
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 250,000 Artrosamin dietary supplement capsules produced from April 2, 2014. The recall follows a consent decree that requires the company to destroy these products under FDA supervision before resuming operations.
The hazard stems from a consent decree that prohibits the company from marketing dietary supplements until they destroy all products made since April 2, 2014. The decree requires destruction under FDA supervision before the company can resume operations.
Owners of Artrosamin capsules manufactured between April 2, 2014, and September 25, 2015 are affected. People using these supplements are at risk due to the company's legal obligation to destroy them.
Check for Artrosamin capsules with lot numbers 030414 through 120514, all expiring on April 17 or May 17, 2014.
Immediately stop using Artrosamin capsules with lot numbers 030414 through 120514.
Sunset Natural Products must destroy these capsules under a consent decree before they can resume operations.
Lots 030414 through 120514, all expiring on April 17 or May 17, 2014.
Check the lot number on the capsule; affected lots are 030414 through 120514 with expiration dates of April 17 or May 17, 2014.
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-0933-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0933-2017 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.
