Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 65725 · Class II · Indiana Blood Center
Key facts
| Event ID | 65725 |
|---|---|
| Recall numbers | B-2511-13 |
| Recalling firm | Indiana Blood Center |
| Product type | Biologics |
| Products | Red Blood Cells (Apheresis) Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, with disparate weights between the two units collected during the apheresis procedure, were distributed. |
| Initiation date | Jun 25, 2013 |
| Report date | Sep 4, 2013 |
| Termination date | Aug 29, 2013 |
| City | Indianapolis |
| State | IN |
| Country | United States |
| FEI number | 1873403 |
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 · Source date: