Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 36698 · Class III · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 36698 |
|---|---|
| Recall numbers | B-0701-7 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman 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 | Oct 17, 2005 |
| 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