Drug recall
Recovered Plasma
FDA recall event 39269 · Class II · LifeShare Blood Centers
Key facts
| Event ID | 39269 |
|---|---|
| Recall numbers | B-1576-08 |
| Recalling firm | LifeShare Blood Centers |
| Product type | Biologics |
| Products | Recovered Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was collected from an unsuitable donor based on risk factors for variant Creutzfeldt-Jakob Disease (vCJD), was distributed |
| Initiation date | May 18, 2007 |
| Termination date | Jun 30, 2008 |
| City | Alexandria |
| State | LA |
| Country | United States |
| FEI number | 2377718 |
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