Sunset Natural Products Inc. recalls Temil dietary supplements made from April 2, 2014, due to a consent decree with FDA requiring destruction. All units 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 Inc. is recalling all Temil dietary supplements manufactured or distributed since April 2, 2014. This recall is required by a consent decree with the FDA to stop the company from marketing supplements until they meet safety standards.
The hazard is that the company violated FDA regulations by marketing dietary supplements without proper oversight. This led to a consent decree requiring the company to stop all sales and destroy all products made since April 2014.
Anyone who owns or used Temil dietary supplements made from April 2, 2014, through September 25, 2015. People who bought these products from any source are at risk.
Check for Temil dietary supplements with a lot number starting with 070315. The products were made between April 2, 2014, and September 25, 2015.
Immediately destroy all Temil dietary supplements with lot number 070315.
Sunset Natural Products Inc. violated FDA regulations and must destroy all products made since April 2, 2014 as part of a consent decree.
Check for Temil dietary supplements with lot number 070315, which were made between April 2, 2014, and September 25, 2015.
Destroy the product immediately under FDA supervision as required by the consent decree.
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-1051-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-1051-2017 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.
