Drug recall
Viapro Capsules Dietary Supplement (Prostancus HCl) 375mg, 1 and 2 count blister cards and 10 count bottles…
FDA recall event 49016 · Class I · EG Labs
Key facts
| Event ID | 49016 |
|---|---|
| Recall numbers | D-138-2009 |
| Recalling firm | EG Labs |
| Product type | Drugs |
| Products | Viapro Capsules Dietary Supplement (Prostancus HCl) 375mg, 1 and 2 count blister cards and 10 count bottles, FOR MEN, Manufactured for: The Male Enhancement Research Center (M.E.R.C.), New York, NY |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unapproved New Drug; product found to contain thio-methisosildenafil, an analog of sildenafil, an unapproved new drug. Sildenafil is the active pharmaceutical used in a FDA approved product for… |
| Initiation date | Jul 23, 2008 |
| Termination date | Oct 28, 2009 |
| City | Odessa |
| State | FL |
| Country | United States |
| FEI number | 3007033102 |
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