Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 33682 · Class III · HemaCare Corporation
Key facts
| Event ID | 33682 |
|---|---|
| Recall numbers | B-0262-6 |
| Recalling firm | HemaCare Corporation |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, associated with units of Platelets that did not meet product specifications, was distributed. |
| Initiation date | Dec 26, 2001 |
| Termination date | Dec 2, 2005 |
| City | Sherman Oaks |
| Country | United States |
| FEI number | 2077774 |
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