Drug recall
Red Blood Cells
FDA recall event 44371 · Class II · LifeServe Blood Center
Key facts
| Event ID | 44371 |
|---|---|
| Recall numbers | B-0743-13 |
| Recalling firm | LifeServe Blood Center |
| Product type | Biologics |
| Products | Red Blood Cells |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, positive for the E-antigen but labeled as E-antigen negative, was distributed. |
| Initiation date | Feb 14, 2007 |
| Report date | Jan 16, 2013 |
| Termination date | Jan 4, 2013 |
| 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: