Sunset Natural Products Inc. recalls Strev bulk capsules manufactured from April 2, 2014, under FDA consent decree requiring destruction. All affected units must be destroyed per 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 all Strev bulk capsules made from April 2, 2014, due to a consent decree with the FDA. This recall requires destroying the products to comply with regulatory requirements.
The hazard stems from a consent decree that prohibits the company from marketing dietary supplements until they comply with FDA regulations. The company must recall and destroy all products manufactured or distributed since April 2, 2014, to meet regulatory requirements.
All owners of Strev bulk capsules manufactured between April 2, 2014, and September 25, 2015, are affected. Consumers who have these products are at risk of regulatory non-compliance.
Check for Strev bulk capsules with lot number 040614 and expiration date July 17, 2017. Products manufactured between April 2, 2014, and September 25, 2015, are affected.
Destroy all Strev bulk capsules with lot number 040614 and expiration date 07/17.
Sunset Natural Products Inc. must recall and destroy these products to comply with a consent decree with the FDA that prohibits marketing dietary supplements until they meet regulatory requirements.
Affected products have lot number 040614 and expiration date 07/17.
The recall was issued on September 25, 2015, per the consent decree.
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-0987-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0987-2017 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.
