Drug recall
Recovered Plasma
FDA recall event 31799 · Class II · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 31799 |
|---|---|
| Recall numbers | B-1204-5, B-1205-5 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman Center |
| Product type | Biologics |
| Products | Recovered Plasma, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products collected from an unsuitable donor due to a history of travel to an area considered at increased risk of exposure to variant Creutzfeldt-Jakob Disease (vCJD)., Blood products collected from an unsuitble donor due to a history of travel to an area considered at increased risk of exposure to variant Creutzfeldt-Jakob disease (vCJD). |
| Initiation date | May 14, 2003 |
| Termination date | May 19, 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