Recall company profile

Bethel Nutritional Consulting, Inc. Recalls

Overview of recall records associated with Bethel Nutritional Consulting, Inc., including dates, categories and classifications where available.

3recall records
Dec 25, 2013latest record date
Sep 4, 2013earliest record date

Recall history in this database

Classification mix: Class I: 3.

DrugDec 25, 2013

Bethel Advance recall — FDA D-372-2014

Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of phenolphthalein, N-di-Desmethylsibutramine, and trace amounts of sibutramine and N-Desmethylsibutramine.…

Class IFDA: TerminatedBethel Nutritional Consulting, Inc.
DrugSep 4, 2013

Bethel 30 capsules recall — FDA D-921-2013

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…

Class IFDA: TerminatedBethel Nutritional Consulting, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Bethel Nutritional Consulting, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.