Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 31880 · Class III · Blood Systems, Inc
Key facts
| Event ID | 31880 |
|---|---|
| Recall numbers | B-1317-5 |
| Recalling firm | Blood Systems, Inc |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, that was labeled as leukoreduced but failed quality control testing due to an elevated white blood cell count, was distributed. |
| Initiation date | Sep 5, 2002 |
| Termination date | Jun 6, 2005 |
| City | Fort Smith |
| Country | United States |
| FEI number | 2371453 |
At a glance
- 1–9 Products in this recall
- None 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