Drug recall
Apheresis Fresh Frozen Plasma
FDA recall event 98450 · Class II · American National Red Cross, Penn Jersey Region
Key facts
| Event ID | 98450 |
|---|---|
| Recall numbers | B-0031-2026, B-0032-2026, B-0033-2026, B-0034-2026, B-0035-2026, B-0036-2026, B-0037-2026, B-0038-2026, B-0039-2026 |
| Recalling firm | American National Red Cross, Penn Jersey Region |
| Product type | Biologics |
| Products | Apheresis Fresh Frozen Plasma, Apheresis Red Blood Cells, Leukocytes Reduced, Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated, Cryoprecipitated AHF, PF24 Plasma and 4 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Apheresis Fresh Frozen Plasma, collected in a manner that compromises the sterility of the collection system, were distributed., Apheresis Red Blood Cells, Leukocytes Reduced, collected in a manner that compromises the sterility of the collection system, were distributed., Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated, collected in a manner that compromises the sterility of the… |
| Initiation date | Apr 3, 2024 |
| Report date | Apr 1, 2026 |
| Termination date | Mar 23, 2026 |
| City | Philadelphia |
| State | PA |
| Country | United States |
| FEI number | 2573021 |
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: