Drug recall
Granulocytes Pheresis
FDA recall event 46548 · Class III · American National Red Cross (The)
Key facts
| Event ID | 46548 |
|---|---|
| Recall numbers | B-0821-13, B-0822-13, B-0823-13, B-0824-13, B-0825-13 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Granulocytes Pheresis, Platelets Pheresis Leukocytes Reduced, Platelets Pheresis Leukocytes Reduced Irradiated, Red Blood Cells, Red Blood Cells-Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, in which QC was not performed or unacceptable for West Nile Virus, were distributed. |
| Initiation date | Nov 8, 2007 |
| Report date | Feb 20, 2013 |
| Termination date | Feb 13, 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: