Drug recall
Apheresis PF24RT24 Plasma
FDA recall event 97214 · Class II · American National Red Cross
Key facts
| Event ID | 97214 |
|---|---|
| Recall numbers | B-0392-2025 |
| Recalling firm | American National Red Cross |
| Product type | Biologics |
| Products | Apheresis PF24RT24 Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Apheresis PF24RT24 Plasma, which did not meet the acceptable targeted plasma volume, was distributed. |
| Initiation date | Aug 19, 2024 |
| Report date | Jul 23, 2025 |
| Termination date | Jul 16, 2025 |
| City | Columbus |
| State | OH |
| Country | United States |
| FEI number | 1573013 |
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: