Drug recall
PF24 Plasma
FDA recall event 94010 · Class II · Versiti Wisconsin, Inc
Key facts
| Event ID | 94010 |
|---|---|
| Recall numbers | B-0139-2024 |
| Recalling firm | Versiti Wisconsin, Inc |
| Product type | Biologics |
| Products | PF24 Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood product identified as unsuitable due to a reactive screening test for transfusion-transmitted infection, was distributed. |
| Initiation date | Nov 22, 2023 |
| Report date | Feb 28, 2024 |
| Termination date | Feb 20, 2024 |
| City | Milwaukee |
| State | WI |
| Country | United States |
| FEI number | 2171378 |
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: