Bethel Nutritional Consulting, Inc recalls Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
Recalled September 4, 2013 · FDA recall D-921-2013 · Bethel Nutritional Consulting
Hazard
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. · FDA Class I
Units
18,678 bottles
Sold at
Nationwide. Product was also available for sale via internet
Description
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.
Product
Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
Manufacturer(s)
Bethel Nutritional Consulting, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →