Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Bethel 30 capsules Recalled by Bethel Nutritional Consulting, Inc Due to Undeclared Sibutramine
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bethel Nutritional Consulting, Inc directly.
Affected Products
Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
Quantity: 18,678 bottles
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bethel Nutritional Consulting, Inc
Bethel Nutritional Consulting, Inc has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report