Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 80936 · Class II, Class III · LifeServe Blood Center
Key facts
| Event ID | 80936 |
|---|---|
| Recall numbers | B-0012-2019, B-0013-2019, B-0014-2019 |
| Recalling firm | LifeServe Blood Center |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Pooled Cryoprecipitated AHF, Red Blood Cells, Leukocytes Reduced, Irradiated |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed. |
| Initiation date | Jun 11, 2018 |
| Report date | Oct 24, 2018 |
| Termination date | Oct 12, 2018 |
| 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: