Sunset Natural Products Inc. recalls Venocell bulk capsules manufactured from April 2, 2014 onward 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 all Venocell bulk capsules made from April 2, 2014 onward because they must destroy these products under a federal consent decree with the FDA. This recall is required to comply with FDA regulations after the company was found to have violated dietary supplement manufacturing standards.
The hazard comes from a federal consent decree that requires the company to destroy all products made after April 2, 2014. This recall is a compliance action with the FDA, not a safety issue with the product itself.
Anyone who purchased or has Venocell bulk capsules made between April 2, 2014 and September 25, 2015. People using these supplements for dietary purposes are most at risk.
Check for lot numbers starting with 370414 or 510414 with expiration dates of April 17, 2014. Products manufactured from April 2, 2014 onward are affected.
Venocell bulk capsules with lot numbers 370414 or 510414 and expiration date April 17, 2014 must be destroyed under FDA supervision.
This recall is required by a federal consent decree that mandates Sunset Natural Products Inc. to destroy all dietary supplements manufactured from April 2, 2014 onward to comply with FDA regulations.
Venocell bulk capsules with lot numbers 370414 or 510414 and expiration date April 17, 2014.
No additional action is required beyond destroying the affected products under FDA supervision.
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-1003-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-1003-2017 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.
