Drug recall
Cryoprecipitated AHF
FDA recall event 95263 · Class III · Vitalant
Key facts
| Event ID | 95263 |
|---|---|
| Recall numbers | B-0487-2024 |
| Recalling firm | Vitalant |
| Product type | Biologics |
| Products | Cryoprecipitated AHF |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Cryoprecipitated AHF, collected from a donor who had limited English language skills, was distributed. |
| Initiation date | Jul 11, 2024 |
| Report date | Oct 2, 2024 |
| Termination date | Sep 23, 2024 |
| City | Denver |
| State | CO |
| Country | United States |
| FEI number | 3000210247 |
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: