Drug recall
Apheresis PF24 Plasma
FDA recall event 91590 · Class II · OneBlood, Inc.
Key facts
| Event ID | 91590 |
|---|---|
| Recall numbers | B-0448-2023, B-0449-2023 |
| Recalling firm | OneBlood, Inc. |
| Product type | Biologics |
| Products | Apheresis PF24 Plasma, Apheresis Platelets, PAS, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood products, possibly contaminated with air, were distributed. |
| Initiation date | Sep 7, 2022 |
| Report date | Feb 8, 2023 |
| Termination date | Feb 1, 2023 |
| City | St Petersburg |
| State | FL |
| Country | United States |
| FEI number | 1070196 |
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: