Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 95292 · Class II · LifeStream Blood Bank
Key facts
| Event ID | 95292 |
|---|---|
| Recall numbers | B-0491-2024, B-0492-2024, B-0493-2024 |
| Recalling firm | LifeStream Blood Bank |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Apheresis Platelets, Leukocytes Reduced, Irradiated, Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood Products, which were labeled as leukocytes reduced but were not tested to verify white blood cell count, were distributed. |
| Initiation date | Feb 18, 2024 |
| Report date | Oct 2, 2024 |
| Termination date | Sep 23, 2024 |
| City | San Bernardino |
| State | CA |
| Country | United States |
| FEI number | 2074143 |
At a glance
- 1–9 Products in this recall
- None 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: