Drug recall
Apheresis PF24 Plasma
FDA recall event 89281 · Class II · American Natl. Red Cross-Greater Chesapeake & Potomac Region
Key facts
| Event ID | 89281 |
|---|---|
| Recall numbers | B-0124-2022 |
| Recalling firm | American Natl. Red Cross-Greater Chesapeake & Potomac Region |
| Product type | Biologics |
| Products | Apheresis PF24 Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood products, collected from a donor for whom donor suitability was not adequately determined, were distributed |
| Initiation date | Jul 24, 2021 |
| Report date | Dec 29, 2021 |
| Termination date | Dec 23, 2021 |
| City | Baltimore |
| State | MD |
| Country | United States |
| FEI number | 1173011 |
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: