MODERATE RISK
Terminated
F-1017-2017
Yohimbe Dietary Supplement (unknown container size)
Recalled by Sunset Natural Products Inc.
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
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 Details
Product Quantity
Unknown
Product Type
Food
Code Info
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 d
Voluntary/Mandated
FDA Mandated
Distribution & Geography
Distribution Pattern
Products distributed to Florida, Nevada and the Dominican Republic
Company Location
Miami, FL, 33155-4509
Timeline
Report Date
01/04/2017
Recall Initiated
10/13/2015
Classification Date
12/28/2016
Termination Date
04/10/2017
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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