Sunset Natural Products recalls Abee Med dietary supplements manufactured since April 2, 2014 due to a consent decree with FDA. Affected products include specific lot numbers and expiration dates.
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 manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Sunset Natural Products is recalling Abee Med dietary supplements made on or after April 2, 2014. This recall follows a consent decree requiring the company to stop marketing supplements until they meet FDA safety standards.
The hazard is tied to a consent decree that prohibits the company from marketing supplements until they fix FDA compliance issues. This means the products may not meet safety standards, but the exact risk isn't specified in the recall notice.
Owners of Abee Med supplements purchased since April 2, 2014 are affected. People who have used these products are at risk due to the company's legal restrictions.
Check for the product name 'Abee Med' with 60 capsules per bottle. Look for lot number 420415, expiration date 04/18, and UPC 850993004017 on the label.
Identify the product by checking the lot number, expiration date, and UPC code on the label.
The company is under a consent decree with the FDA that requires them to stop marketing supplements until they meet safety standards.
The recall notice does not specify a remedy, so check the product details and contact the manufacturer for further instructions.
The product was manufactured on or after April 2, 2014.
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-0536-2016 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-0536-2016 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.
