Drug recall
Platelets Pheresis, Leukocyte Reduced Irradiated
FDA recall event 33785 · Class III · American Red Cross Blood Services
Key facts
| Event ID | 33785 |
|---|---|
| Recall numbers | B-0524-6 |
| Recalling firm | American Red Cross Blood Services |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocyte Reduced Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, labeled as leukoreduced but not tested for white blood cell (WBC) count as required, was distributed. |
| Initiation date | Jun 24, 2005 |
| Termination date | Jan 23, 2006 |
| City | Columbus |
| Country | United States |
| FEI number | 1573013 |
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