Sunset Natural Products Inc. recalls Bionix dietary supplements manufactured from April 2, 2014, due to a consent decree with FDA requiring destruction. All affected lots 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 Bionix dietary supplements made from April 2, 2014, because they violated FDA regulations. The company must destroy all recalled products under FDA supervision as part of a consent decree.
The hazard stems from the company's violation of FDA regulations, which led to a consent decree requiring destruction of all affected products. The company must destroy these supplements under FDA supervision to comply with the decree.
All owners of Bionix dietary supplements manufactured between April 2, 2014, and September 25, 2015, are affected. Consumers who have these products are at risk of potential regulatory violations.
Check for Bionix dietary supplements with lot numbers 380414 (expiring April 17), 310614 (expiring July 17), or 391014 (expiring December 17).
Destroy all recalled Bionix supplements under FDA supervision as required by the consent decree.
Sunset Natural Products Inc. violated FDA regulations, leading to a consent decree that requires destruction of all affected products.
Lots 380414 (expiring April 17), 310614 (expiring July 17), and 391014 (expiring December 17).
Check the lot number and expiration date on the product label.
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-0909-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0909-2017 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.
