Sunset Natural Products Inc. recalls Foni bulk capsules manufactured from April 2, 2014, due to FDA consent decree 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 Foni bulk capsules made from April 2, 2014, because they violated FDA regulations. The company must destroy all these supplements under FDA supervision as part of a consent decree.
The hazard comes 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.
Anyone who owns or uses Foni bulk capsules manufactured between April 2, 2014, and September 25, 2015. People most at risk are those who have the specific lots mentioned in the recall.
Check for lot numbers 370614 (expiration 06/17) or 170215 (expiration 03/18) on Foni bulk capsules. Products manufactured between April 2, 2014, and September 25, 2015, are affected.
Look for lot numbers 370614 (expiration 06/17) or 170215 (expiration 03/18) on the capsules.
If you have the affected lots, destroy them immediately under FDA supervision as required by the consent decree.
Sunset Natural Products Inc. violated FDA regulations and must destroy all affected products under a consent decree to comply with FDA requirements.
Lot # 370614 (expiration 06/17) and Lot # 170215 (expiration 03/18).
Yes, the company must destroy the products under FDA supervision as part of the recall process.
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-0991-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0991-2017 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.
