CLASS IIFood recall · Reported 4 Jan 2017 · FDA Enforcement Report
Colageina Gold recalled by Sunset Natural Products
Sunset Natural Products is recalling Colageina Gold, distributed in Florida, Nevada. The recall was initiated on 13 Oct 2015 and the FDA has classified it as Class II.
Check your package
Lot, batch or date codesAs persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with the procedures provided in paragraph 6, ALL dietary supplements that were manufactured, prepared, processed, packed, labeled, held and/or distributed between April 2, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lots and expiration dates: Lot # 230514 Exp. Date 06/17, Lot # 330614 Exp. Date 06/17, Lot # 500714 Exp. Date 09/17, Lot # 510714 Exp. Date 10/17, Lot # 520714 Exp. Date 11/17, Lot # 360914 Exp. Date 07/18, Lot # 430814 Exp. Date 08/16, Lot # 450814 Exp. Date 08/14, Lot # 330914 Exp. Date 09/16, Lot # 340914 Exp. Date 09/16, Lot # 350914 Exp. Date 09/16, Lot # 370914 Exp. Date 09/16
Quantity recalled10,663 Jars
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Product as listed by the FDA
Colageina Gold, 195 g Jars
Where it was distributed
Products distributed to Florida, Nevada and the Dominican Republic
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.
Which lots are affected?
As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with the procedures provided in paragraph 6, ALL dietary supplements that were manufactured, prepared, processed, packed, labeled, held and/or distributed between April 2, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lots and expiration dates: Lot # 230514 Exp. Date 06/17, Lot # 330614 Exp. Date 06/17, Lot # 500714 Exp. Date 09/17, Lot # 510714 Exp. Date 10/17, Lot # 520714 Exp. Date 11/17, Lot # 360914 Exp. Date 07/18, Lot # 430814 Exp. Date 08/16, Lot # 450814 Exp. Date 08/14, Lot # 330914 Exp. Date 09/16, Lot # 340914 Exp. Date 09/16, Lot # 350914 Exp. Date 09/16, Lot # 370914 Exp. Date 09/16
Where was it sold?
Products distributed to Florida, Nevada and the Dominican Republic
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.