Drug recall
Source Plasma
FDA recall event 43672 · Class II · PlasmaCare Inc
Key facts
| Event ID | 43672 |
|---|---|
| Recall numbers | B-2009-13 |
| Recalling firm | PlasmaCare Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who did not have a complete physical examination, were distributed. |
| Initiation date | Oct 14, 2006 |
| Report date | Jun 26, 2013 |
| Termination date | Jun 19, 2013 |
| City | Columbus |
| State | OH |
| Country | United States |
| FEI number | 3004498724 |
At a glance
- 1–9 Products in this recall
- 1–9 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: