Drug recall
Apheresis PF24RT24 Plasma
FDA recall event 97114 · Class II · American National Red Cross (The)
Key facts
| Event ID | 97114 |
|---|---|
| Recall numbers | B-0367-2025, B-0368-2025, B-0369-2025, B-0370-2025, B-0371-2025, B-0372-2025 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Apheresis PF24RT24 Plasma, Apheresis Red Blood Cells, Leukocytes Reduced, Liquid Plasma, PF24 Plasma, Red Blood Cells, Leukocytes Reduced and 1 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Apheresis PF24RT24 Plasma, for which Babesia testing was not performed, were distributed., Apheresis Red Blood Cells, Leukocytes Reduced, for which Babesia testing was not performed, were distributed., Liquid Plasma, for which Babesia testing was not performed, was distributed., PF24 Plasma, for which Babesia testing was not performed, was distributed., Red Blood Cells, Leukocytes Reduced, for… |
| Initiation date | May 10, 2023 |
| Report date | Jul 23, 2025 |
| Termination date | Jul 14, 2025 |
| City | Madison |
| State | WI |
| Country | United States |
| FEI number | 2173028 |
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: