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.
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.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Bethel Nutritional Consulting, Inc to request your refund or repair — edit it as you like.
Subject: Recall D-921-2013 — Bethel Nutritional Consulting, Inc Bethel Nutritional Consulting, Inc recalls Bethel 30 capsules, pa Hello, I own a Bethel Nutritional Consulting, Inc recalls Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York that is covered by recall D-921-2013 from Bethel Nutritional Consulting, Inc. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
