Sunset Natural Products recalls Pritos bulk capsules manufactured from April 2014 onward due to FDA compliance violations. Affected products must be destroyed per a consent decree.
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 is recalling all Pritos bulk capsules made from April 2, 2014, because they violated FDA regulations. This recall follows a consent decree requiring the company to destroy these products under FDA supervision.
The hazard comes from the company's violation of FDA regulations, which led to a consent decree requiring the destruction of these products. The products were manufactured and distributed without proper compliance, posing a risk of regulatory non-compliance.
Anyone who owns or uses Pritos bulk capsules made from April 2, 2014, onward. People who have these products are most at risk as they must destroy them per the recall.
Check for Pritos bulk capsules with lot numbers starting with 020415 (expiring May 18) or 080515 (expiring June 18). Products made from April 2, 2014, onward are affected.
Destroy all Pritos bulk capsules with lot numbers 020415 (expiring May 18) or 080515 (expiring June 18) immediately.
Sunset Natural Products violated FDA regulations, leading to a consent decree that requires destroying all products made from April 2, 2014, onward.
Pritos bulk capsules with lot numbers 020415 (expiring May 18) or 080515 (expiring June 18).
The recall requires destroying the products under FDA supervision, not refunds or replacements.
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-1000-2017 — Sunset Natural Products Sunset Natural Products Hello, I own a Sunset Natural Products that is covered by recall F-1000-2017 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.
