Drug recall
Recovered Plasma
FDA recall event 31034 · Class II · LifeShare Blood Centers
Key facts
| Event ID | 31034 |
|---|---|
| Recall numbers | B-0747-5, B-0748-5 |
| Recalling firm | LifeShare Blood Centers |
| 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 a donor who was at increased risk for new variant Creutzfeldt-Jakob Disease (nvCJD), were distributed. |
| Initiation date | Aug 19, 2003 |
| Termination date | Mar 9, 2005 |
| City | Shreveport |
| Country | United States |
| FEI number | 2370879 |
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