Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 33553 · Class III · Belle Bonfils Memorial Blood Center
Key facts
| Event ID | 33553 |
|---|---|
| Recall numbers | B-0370-6 |
| Recalling firm | Belle Bonfils Memorial Blood Center |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were labeled leukoreduced, but had an unacceptable white blood cell count, were distributed. |
| Initiation date | Jan 27, 2000 |
| Termination date | Dec 8, 2005 |
| City | Denver |
| Country | United States |
| FEI number | 3000210247 |
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