Sunset Natural Products Inc.: Food Recall in 2017 - (Recall #: F-0916-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Test Booster, 90 or 60 capsules per bottle

Product Classification:

Class II

Date Initiated: October 13, 2015

Date Posted: January 4, 2017

Recall Number: F-0916-2017

Event ID: 74054

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.

Status: Terminated

Product Quantity: 5292 Bottles (337,000 capsules)

Code Information:

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 # 011114 Exp. Date 11/17, Lot # 010215 Exp. Date 02/18, Lot # 130215 Exp. Date 02/18, Lot # 191014 Exp. Date 10/17

Distribution Pattern:

Products distributed to Florida, Nevada and the Dominican Republic

Voluntary or Mandated:

FDA Mandated