Drug recall
Recovered Plasma
FDA recall event 48861 · Class II, Class III · American Red Cross Blood Services
Key facts
| Event ID | 48861 |
|---|---|
| Recall numbers | B-2435-12, B-2436-12 |
| Recalling firm | American Red Cross Blood Services |
| Product type | Biologics |
| Products | Recovered Plasma, Red Blood Cells Leukocytes Reduced |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed. |
| Initiation date | Jun 5, 2008 |
| Report date | Aug 22, 2012 |
| Termination date | Aug 16, 2012 |
| City | Wichita |
| State | KS |
| Country | United States |
| FEI number | 1973042 |
At a glance
- 1–9 Products in this recall
- 10–99 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: