Drug recall
Pooled Cryoprecipitated AHF
FDA recall event 91472 · Class II · LifeServe Blood Center
Key facts
| Event ID | 91472 |
|---|---|
| Recall numbers | B-0129-2023, B-0130-2023 |
| Recalling firm | LifeServe Blood Center |
| Product type | Biologics |
| Products | Pooled Cryoprecipitated AHF, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood products, for which donor eligibility was incomplete, were distributed. |
| Initiation date | Jul 13, 2022 |
| Report date | Jan 18, 2023 |
| Termination date | Jan 12, 2023 |
| City | Des Moines |
| State | IA |
| Country | United States |
| FEI number | 1970355 |
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: