Drug recall
Platelets Pheresis Leukoreduced
FDA recall event 32872 · Class II · Regional Health Resource Center
Key facts
| Event ID | 32872 |
|---|---|
| Recall numbers | B-2238-5, B-2239-5, B-2240-5 |
| Recalling firm | Regional Health Resource Center |
| Product type | Biologics |
| Products | Platelets Pheresis Leukoreduced, Red Blood Cells, Red Blood Cells Leukoreduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, tested for anti-HBc using an expired reagent, were distributed. |
| Initiation date | May 5, 2005 |
| Termination date | Oct 21, 2005 |
| City | Urbana |
| Country | United States |
| FEI number | 1470270 |
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