Project #3, 60 capsules per bottle

Sunset Natural Products INC. recalled Project #3, 60 capsules per bottle in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Oct 13, 2015.

The FDA-published reason for this recall is: "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."

The product reached multiple states, recorded by the FDA as "Products distributed to Florida, Nevada and the Dominican Republic." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Miami, FL. The recall covers 1940 Bottles (120,000 capsules) of product. The FDA has Terminated this recall (first reported Jan 4, 2017), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.