Drug recall
Fresh Frozen Plasma
FDA recall event 32418 · Class III · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 32418 |
|---|---|
| Recall numbers | B-0253-6, B-0254-6, B-0255-6, B-0256-6, B-0257-6 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman Center |
| Product type | Biologics |
| Products | Fresh Frozen Plasma, Fresh Frozen Plasma (Apheresis), Platelets Pheresis, Irradiated, Platelets Pheresis, Leukocytes Reduced, Red Blood Cells, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, incorrectly tested for West Nile Virus (WNV), were distributed. |
| Initiation date | Mar 30, 2004 |
| Termination date | Dec 9, 2005 |
| 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