Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York

Recall Number: D-921-2013

Firm: Bethel Nutritional Consulting, Inc

Classification: Class I

Status: Terminated

Report Date: 20130904

Initiation Date: 20130611

Termination Date: 20180627

Marketed Without An Approved NDA/ANDA: FDA analysis found this product contained undeclared sibutramine and phenolphthalein, two active ingredients that were once marketed in the U.S. but removed due to safety reasons, making this product an unapproved new drug.

Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York