Drug recall
Reversitol Dietary Supplement Capsules, 624mg proprietary blend, 60 capsules/bottle, Anti-Aromatase…
FDA recall event 57316 · Class I · Tribravus Enterprises, Llc
Key facts
| Event ID | 57316 |
|---|---|
| Recall numbers | D-430-2011 |
| Recalling firm | Tribravus Enterprises, Llc |
| Product type | Drugs |
| Products | Reversitol Dietary Supplement Capsules, 624mg proprietary blend, 60 capsules/bottle, Anti-Aromatase, Testosterone, Mfg For Dist. By Tribravus Enterprises, LLC, Escondido, CA - UPC 8 5450300113 8 |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Marketed Without an Approved NDA/ANDA; product contains 6-Etioallochol-1,4-Diene-3,17-Dione which is a synonym of ATD. ATD is classified as an aromatase inhibitor |
| Initiation date | Sep 16, 2010 |
| Termination date | Jul 9, 2014 |
| City | Vista |
| State | CA |
| Country | United States |
| FEI number | 3008549556 |
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