Drug recall
Fresh Frozen Plasma (Apheresis)
FDA recall event 39842 · Class II · American Red Cross Blood Services
Key facts
| Event ID | 39842 |
|---|---|
| Recall numbers | B-1646-13, B-1647-13 |
| Recalling firm | American Red Cross Blood Services |
| Product type | Biologics |
| Products | Fresh Frozen Plasma (Apheresis), Platelets Pheresis Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from an unsuitable donor based on risk factors for variant Creutzfeldt-Jakob Disease (vCJD), were distributed. |
| Initiation date | Feb 25, 2005 |
| Report date | May 8, 2013 |
| Termination date | Apr 29, 2013 |
| City | Omaha |
| State | NE |
| Country | United States |
| FEI number | 1973037 |
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: