PlainRecalls
FDA Drug Critical Class I Terminated

SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.

Reported: July 15, 2015 Initiated: December 19, 2014 #D-1207-2015

Product Description

SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.

Reason for Recall

Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.

Details

Units Affected
UNKNOWN
Distribution
Nationwide
Location
New York, NY

Frequently Asked Questions

What product was recalled?
SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.. Recalled by Bethel Nutritional Consulting, Inc. Units affected: UNKNOWN.
Why was this product recalled?
Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 15, 2015. Severity: Critical. Recall number: D-1207-2015.