Sunset Natural Products recalls Magnun Plus supplements manufactured from April 2014 onward due to a consent decree with FDA. Consumers must destroy all recalled products.
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 all Magnun Plus dietary supplements made since April 2, 2014. This recall follows a consent decree requiring the company to destroy these products under FDA supervision.
The hazard is not described in the recall notice. The company is under a consent decree with the FDA that requires them to destroy these products, but the specific safety risk is not stated.
Anyone who owns or uses Magnun Plus supplements made from April 2, 2014 onward. People who have these products are most at risk.
Check for Magnun Plus supplements with lot numbers 210514 (expiring May 17) or 050315 (expiring March 18). Products made after April 2, 2014 are also affected.
Sunset Natural Products requires consumers to destroy all recalled Magnun Plus supplements under FDA supervision.
The company is under a consent decree with the FDA that requires them to destroy these products. The specific safety risk is not stated in the recall notice.
Magnun Plus supplements made from April 2, 2014 onward, including lot numbers 210514 (expiring May 17) and 050315 (expiring March 18).
Check the lot number and expiration date on the product. Products with lot numbers 210514 (expiring May 17) or 050315 (expiring March 18) are affected.
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-0939-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0939-2017 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.
