Drug recall
Recovered Plasma
FDA recall event 33835 · Class II · American National Red Cross, The
Key facts
| Event ID | 33835 |
|---|---|
| Recall numbers | B-0456-6, B-0457-6 |
| Recalling firm | American National Red Cross, The |
| 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 of variant Creutzfeldt Jakob Disease (vCJD), were distributed. |
| Initiation date | Jun 28, 2002 |
| Termination date | Jan 12, 2006 |
| City | Pomona |
| Country | United States |
| FEI number | 2072994 |
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