Sunset Natural Products Inc. recalls Abte bulk capsules manufactured from April 2, 2014, under FDA consent decree requiring destruction of all affected 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 Inc. is recalling Abte bulk capsules made from April 2, 2014, because they violated FDA regulations. This recall is part of a consent decree requiring the company to destroy all affected products before resuming operations.
The company violated FDA regulations by marketing dietary supplements without proper compliance. This led to a consent decree requiring them to recall and destroy all affected products before they could resume operations.
Anyone who owns or uses Abte bulk capsules manufactured between April 2, 2014, and September 25, 2015. The risk is highest for consumers who have these products.
Check for Abte bulk capsules with lot number 040714 and expiration date July 17, 2017. Products manufactured between April 2, 2014, and September 25, 2015, are affected.
Immediately stop using Abte bulk capsules with lot number 040714 and expiration date 07/17.
Sunset Natural Products Inc. violated FDA regulations and must destroy all affected products under a consent decree before resuming operations.
Lot number 040714 with expiration date July 17, 2017.
The recall was issued on September 25, 2015, when the consent decree was entered.
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-0993-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0993-2017 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.
