Sunset Natural Products is recalling Project #2 dietary supplements manufactured from April 2, 2014, due to a consent decree with the FDA requiring destruction of all 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 Project #2 dietary supplements (90 capsules per bottle) made from April 2, 2014, because the company violated FDA regulations and must destroy these products under a consent decree.
The company violated FDA regulations by marketing dietary supplements without proper oversight. This led to a consent decree requiring the destruction of all products made since April 2, 2014, to prevent further regulatory violations.
Anyone who owns or uses Project #2 dietary supplements manufactured between April 2, 2014, and September 25, 2015. People who have these products are most at risk.
Look for Project #2 dietary supplements with lot number 011014 and expiration date 10/17. These products were manufactured between April 2, 2014, and September 25, 2015.
Immediately destroy all Project #2 dietary supplements with lot number 011014 and expiration date 10/17.
Sunset Natural Products violated FDA regulations and must destroy all Project #2 supplements made since April 2, 2014, as part of a consent decree.
Check for lot number 011014 and expiration date 10/17 on Project #2 dietary supplements manufactured between April 2, 2014, and September 25, 2015.
Destroy the product immediately as part of the recall process.
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-0912-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0912-2017 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.
