Sunset Natural Products recalls Triflex dietary supplements made from April 2014 to September 2015 due to FDA consent decree requirements. Consumers should 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 Triflex dietary supplements made between April 2014 and September 2015. This recall is required by a court order to comply with FDA regulations after the company violated food safety laws.
The company violated FDA food safety regulations and was ordered to stop selling supplements until they meet strict compliance requirements. The recall is a legal requirement to destroy products made during this period.
Anyone who purchased Triflex dietary supplements between April 2014 and September 2015. People who have the recalled products are most at risk.
Check for lot numbers 350414, 171014, 251214, or 170115 on the container. The product was sold between April 2, 2014 and September 25, 2015.
Immediately destroy all Triflex dietary supplements with lot numbers 350414, 171014, 251214, or 170115.
Sunset Natural Products violated FDA food safety regulations and was ordered to stop selling supplements until they meet compliance requirements.
Lot numbers 350414, 171014, 251214, and 170115.
The product was made 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-1077-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-1077-2017 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.
