Drug recall
Cryoprecipitated AHF
FDA recall event 95689 · Class II · ImpactLife
Key facts
| Event ID | 95689 |
|---|---|
| Recall numbers | B-0085-2025 |
| Recalling firm | ImpactLife |
| Product type | Biologics |
| Products | Cryoprecipitated AHF |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Cryoprecipitated AHF, for which donor eligibility screening was incomplete, were distributed. |
| Initiation date | Sep 18, 2024 |
| Report date | Nov 27, 2024 |
| Termination date | Nov 15, 2024 |
| City | Davenport |
| State | IA |
| Country | United States |
| FEI number | 1970356 |
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: