Sunset Natural Products Inc. recalls 50,000 Argindione capsules manufactured from April 2, 2014, due to FDA consent decree requiring destruction. All affected products must be destroyed 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 50,000 Argindione dietary supplement capsules made between April 2, 2014 and September 25, 2015. This recall follows a consent decree with the FDA that requires the company to destroy all affected products under FDA supervision.
The product was recalled due to a consent decree from the FDA that prohibits the company from marketing dietary supplements until they destroy all affected products and meet regulatory requirements. The hazard is not a physical risk to users but a legal requirement to destroy the product under FDA supervision.
Owners of Argindione capsules with lot number 520414 and expiration date April 17, 2017 are affected. The recall covers products distributed since April 2, 2014.
Check for lot number 520414 and expiration date April 17, 2017 on the product packaging. The recall covers capsules distributed between April 2, 2014 and September 25, 2015.
Destroy all Argindione capsules with lot number 520414 and expiration date April 17, 2017 under FDA supervision.
This product is being recalled due to a consent decree with the FDA that requires Sunset Natural Products to destroy all affected products before resuming supplement sales.
The specific lot number is 520414 with an expiration date of April 17, 2017.
Check for lot number 520414 and expiration date April 17, 2017 on the product packaging. The recall covers capsules distributed between April 2, 2014 and September 25, 2015.
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-0935-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0935-2017 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.
