Drug recall
Platelet, pheresis Leukoreduced
FDA recall event 25434 · Class II · Blood Bank Of Delaware Inc
Key facts
| Event ID | 25434 |
|---|---|
| Recall numbers | B-0644-3 |
| Recalling firm | Blood Bank Of Delaware Inc |
| Product type | Biologics |
| Products | Platelet, pheresis Leukoreduced |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were below the firm's specification for product volume, were distributed. |
| Initiation date | Nov 28, 2001 |
| City | Newark |
| Country | United States |
| FEI number | 2577603 |
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