Drug recall
Pooled Cryoprecipitated AHF
FDA recall event 93588 · Class III · Versiti Illinois Inc
Key facts
| Event ID | 93588 |
|---|---|
| Recall numbers | B-0092-2024 |
| Recalling firm | Versiti Illinois Inc |
| Product type | Biologics |
| Products | Pooled Cryoprecipitated AHF |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood product, not meeting product specifications, was distributed. |
| Initiation date | Oct 12, 2023 |
| Report date | Dec 27, 2023 |
| Termination date | Dec 19, 2023 |
| City | Aurora |
| State | IL |
| Country | United States |
| FEI number | 1470274 |
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: