Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 95533 · Class II · Vitalant
Key facts
| Event ID | 95533 |
|---|---|
| Recall numbers | B-0032-2025 |
| Recalling firm | Vitalant |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Leukoreduced Apheresis Red Blood Cells, which were determined to have low actual RBC volume and failed quality control, were distributed. |
| Initiation date | Jul 26, 2024 |
| Report date | Nov 6, 2024 |
| Termination date | Oct 25, 2024 |
| City | El Paso |
| State | TX |
| Country | United States |
| FEI number | 1671451 |
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: