Drug recall
PF24 Plasma
FDA recall event 99501 · Class III · The American National Red Cross
Key facts
| Event ID | 99501 |
|---|---|
| Recall numbers | B-0163-2026, B-0164-2026, B-0165-2026 |
| Recalling firm | The American National Red Cross |
| Product type | Biologics |
| Products | PF24 Plasma, Red Blood Cells, Leukocytes Reduced, Red Blood Cells, Leukocytes Reduced, Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | PF24 Plasma, collected from donors whose arm inspections were not properly performed, were distributed., Red Blood Cells, Leukocytes Reduced, collected from donors whose arm inspections were not properly performed, were distributed., Red Blood Cells, Leukocytes Reduced, Irradiated, collected from donors whose arm inspections were not properly performed, were distributed. |
| Initiation date | Apr 29, 2025 |
| Report date | Sep 16, 2026 |
| Termination date | Sep 8, 2026 |
| City | Cleveland |
| State | OH |
| Country | United States |
| FEI number | 1573019 |
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: