Drug recall
Recovered Plasma
FDA recall event 29260 · Class III · American National Red Cross SW Region
Key facts
| Event ID | 29260 |
|---|---|
| Recall numbers | B-1555-4 |
| Recalling firm | American National Red Cross SW Region |
| Product type | Biologics |
| Products | Recovered Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product collected from an unsuitable donor due to a history of travel to an area considered at increased risk of exposure to new variant Creutzfeldt-Jakob Disease (nvCJD). |
| Initiation date | Jul 1, 2002 |
| Termination date | Jul 20, 2004 |
| City | Tulsa |
| Country | United States |
| FEI number | 1673040 |
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