Drug recall
Apheresis Platelets, Leukocytes Reduced, Irradiated
FDA recall event 95692 · Class II · Versiti Wisconsin, Inc
Key facts
| Event ID | 95692 |
|---|---|
| Recall numbers | B-0088-2025 |
| Recalling firm | Versiti Wisconsin, Inc |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Leukoreduced Apheresis Platelets, Irradiated, which were returned at an unacceptible temperature, were distributed. |
| Initiation date | Oct 2, 2024 |
| Report date | Nov 27, 2024 |
| Termination date | Nov 15, 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: