Ultimate Body Tox recalls Ultimate Body Tox PRO capsules, Proprietary Blend, 350 mg, 45 count bottle, Manufactured for: JSN Health, 305 Broadway,
Ultimate Body Tox PRO capsules (350mg, 45-count) were recalled due to undeclared sibutramine, a controlled substance removed from the U.S. market in 2010. Safety and efficacy not established for this unapproved drug.
Recall notice
Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine. The presence of sibutramine, a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons, in this tainted product renders it an unapproved drug for which safety and efficacy have not been established and therefore subject to recall.
Contact the company & request your remedy
What happened, in plain English
Ultimate Body Tox PRO capsules (350mg, 45-count) were recalled because they contain undeclared sibutramine, a controlled substance banned in the U.S. since 2010. This makes the product unapproved and potentially unsafe without proper regulatory review. Read more at govinfonow.com/recall/42254-ultimate-body-tox-pro-capsules-recalled-unapproved-drug-with-undeclared.
Source Summary by GovInfoNow · govinfonow.com/recall/42254-ultimate-body-tox-pro-capsules-recalled-unapproved-drug-with-undeclared · Updated October 8, 2026 · FDA enforcement record: FDA #D-0210-2017
Cite this page
“Ultimate Body Tox PRO capsules recalled: Unapproved drug with undeclared sibutramine.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/42254-ultimate-body-tox-pro-capsules-recalled-unapproved-drug-with-undeclared. Based on FDA recall #D-0210-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0210-2017%22&limit=1).
Why it’s dangerous
The capsules contain sibutramine, a controlled substance that was removed from the U.S. market in 2010 for safety reasons. Since this product lacks FDA approval, its safety and effectiveness have not been verified, creating potential health risks.
Who’s affected
People who purchased Ultimate Body Tox PRO capsules (350mg, 45-count) from retailers. Those with medical conditions or using weight loss products may be at higher risk due to the unapproved substance.
How to tell if you have this one
Check for Ultimate Body Tox PRO capsules labeled 350 mg, 45 count, manufactured for JSN Health at 305 Broadway, New York, NY 10007. All lots and manufacturing dates are included in the recall.
- Brand
Ultimate Body Tox- Category
Drug
What to do — step by step
Check Product Details
Verify the product label matches Ultimate Body Tox PRO capsules (350 mg, 45 count) manufactured for JSN Health at 305 Broadway, New York, NY 10007.
Questions people ask
Why was this product recalled?
The product contains undeclared sibutramine, a controlled substance removed from the U.S. market in 2010. This makes it an unapproved drug with unverified safety and efficacy.
Is this product safe to use?
No, the product is unapproved and contains sibutramine, which was banned in the U.S. for safety reasons in 2010. Safety and effectiveness have not been established.
What should I do if I have this product?
The recall record does not specify a remedy, so check the product details and contact the manufacturer if you have concerns.
Contact Ultimate Body Tox
We’ve drafted a message you can send Ultimate Body Tox to request your refund or repair — edit it as you like.
Subject: Recall D-0210-2017 — Ultimate Body Tox Ultimate Body Tox Hello, I own a Ultimate Body Tox that is covered by recall D-0210-2017 from Ultimate Body Tox. 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.
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Where this comes from
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.
- Official source: FDA Recall #D-0210-2017 (November 13, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0210-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.