Drug recall
Apheresis Platelets, Leukocytes Reduced, Irradiated
FDA recall event 96522 · Class III · Versiti Wisconsin, Inc
Key facts
| Event ID | 96522 |
|---|---|
| Recall numbers | B-0245-2025 |
| Recalling firm | Versiti Wisconsin, Inc |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Leukoreduced, Apheresis Platelets, Irradiated, shipped without documentation of acceptable temperature, were distributed. |
| Initiation date | Sep 27, 2024 |
| Report date | Apr 23, 2025 |
| Termination date | Apr 15, 2025 |
| 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: