Drug recall
Recovered Plasma
FDA recall event 28518 · Class II · American Red Cross Blood Serv
Key facts
| Event ID | 28518 |
|---|---|
| Recall numbers | B-1075-4 |
| Recalling firm | American Red Cross Blood Serv |
| Product type | Biologics |
| Products | Recovered Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor who is considered at increased risk of exposure to Creutzfeldt-Jakob Diesease (vCJD), was distributed. |
| Initiation date | Dec 17, 2002 |
| Termination date | Apr 28, 2004 |
| City | Boise |
| Country | United States |
| FEI number | 3072990 |
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