Class IITerminated in FDA datasetOct 13, 2015

H-Stane, 60 capsules per bottle

Recalling firm: Sunset Natural Products Inc.

Why it was recalled

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.

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The exact product

H-Stane, 60 capsules per bottle

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

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Original FDA 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 lot and expiration date: Lot # 170515 Exp. Date 05/18

TypeCode / valueContext
lot170515cree was entered on September 25, 2015. Known lot and expiration date: Lot # 170515 Exp. Date 05/18

Recall details

Recall number
F-0922-2017
Event ID
74054
FDA status
Terminated
Initiated
Oct 13, 2015
Reported
Jan 4, 2017
Classified
Dec 28, 2016
Terminated
Apr 10, 2017
Quantity
500 Bottles, (30,000 capsules)
Location
Miami, FL, United States
Initiation type
FDA Mandated
Notification
Letter

Where it was distributed

Products distributed to Florida, Nevada and the Dominican Republic

FDA source record · F-0922-2017

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.