Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 36808 · Class II · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 36808 |
|---|---|
| Recall numbers | B-0658-7 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman Center |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Platelets, which were incorrectly labeled as leukoreduced products, were distributed. |
| Initiation date | Jun 6, 2006 |
| Termination date | Feb 2, 2007 |
| City | Oklahoma City |
| Country | United States |
| FEI number | 1626009 |
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