Drug recall
Fresh Frozen Plasma Pheresis
FDA recall event 37239 · Class II · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 37239 |
|---|---|
| Recall numbers | B-0821-7, B-0822-7, B-0823-7, B-0824-7 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman Center |
| Product type | Biologics |
| Products | Fresh Frozen Plasma Pheresis, Recovered Plasma, Red Blood Cells, Red Blood Cells Pheresis, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from an ineligible donor due to a history of a hepatitis and jaundice, were distributed., Blood products, collected from an ineligible donor due to a history of a hepatitis and jaundice, were distributed.. |
| Initiation date | Nov 16, 2005 |
| Termination date | Mar 7, 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