Drug recall
Apheresis Platelets, Leukocytes Reduced, Irradiated
FDA recall event 96141 · Class II · New York Blood Center Inc
Key facts
| Event ID | 96141 |
|---|---|
| Recall numbers | B-0148-2025 |
| Recalling firm | New York Blood Center Inc |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Apheresis Platelets Products, for which documentation of irradiation was incomplete, were distributed. |
| Initiation date | Dec 3, 2024 |
| Report date | Feb 12, 2025 |
| Termination date | Jan 31, 2025 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 2170665 |
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: