Reported Sep 4, 2013 · Terminated
Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
Bethel Nutritional Consulting, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Bethel Nutritional Consulting, Inc · 599 W 190th St Ste 1 · New York, NY · 10040-3577
Is this the product you have?
- Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
- Lot codes and dates
- Lot #: 120514
- EXP12/2014
- Amount recalled
- 18,678 bottles
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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