Drug recall
Plasma
FDA recall event 26219 · Class II · American Natl Red Cross Mid At
Key facts
| Event ID | 26219 |
|---|---|
| Recall numbers | B-1227-3, B-1228-3 |
| Recalling firm | American Natl Red Cross Mid At |
| Product type | Biologics |
| Products | Plasma, Red Blood Cell, Leukocytes Reduced |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from an ineligible donor due to use of the medication Arava, were distributed. |
| Initiation date | Jan 24, 2003 |
| City | Norfolk |
| Country | United States |
| FEI number | 1173024 |
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