Drug recall
Ultimate Body Tox PRO capsules, Proprietary Blend, 350 mg, 45 count bottle, Manufactured for: JSN Health, 305…
FDA recall event 75832 · Class I · Ultimate Body Tox
Key facts
| Event ID | 75832 |
|---|---|
| Recall numbers | D-0210-2017 |
| Recalling firm | Ultimate Body Tox |
| Product type | Drugs |
| Products | Ultimate Body Tox PRO capsules, Proprietary Blend, 350 mg, 45 count bottle, Manufactured for: JSN Health, 305 Broadway, 7th Floor, New York, NY 10007. |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Nov 13, 2016 |
| Report date | Dec 28, 2016 |
| Termination date | Jul 27, 2017 |
| City | Rowland |
| State | NC |
| Country | United States |
| FEI number | 3013014165 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: