Sunset Natural Products is recalling Hecle dietary supplements manufactured from April 2, 2014, under a consent decree requiring destruction to comply with FDA regulations. All affected products must be destroyed per the decree.
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 Hecle dietary supplements made from April 2, 2014, because the company violated FDA rules and must destroy them under a consent decree. This recall affects consumers who bought these supplements during that period.
The company violated FDA regulations by marketing dietary supplements without proper compliance. As a result, the products must be destroyed under a consent decree to prevent further regulatory violations.
Anyone who purchased Hecle dietary supplements between April 2, 2014, and September 25, 2015, is affected. Consumers who bought these products during that timeframe are most at risk.
Check for Hecle dietary supplements with lot numbers 190215 or 250515. Products were manufactured and distributed between April 2, 2014, and September 25, 2015.
Hecle dietary supplements with lot numbers 190215 or 250515 must be destroyed as per the consent decree.
Sunset Natural Products violated FDA regulations and must destroy all Hecle dietary supplements made from April 2, 2014, to comply with a consent decree.
Lot numbers 190215 and 250515 are affected.
Products were manufactured and 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-1047-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-1047-2017 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
