Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 76722 · Class III · LifeServe Blood Center
Key facts
| Event ID | 76722 |
|---|---|
| Recall numbers | B-0437-2017, B-0438-2017 |
| Recalling firm | LifeServe Blood Center |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced, Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Red blood cells, for which quality control testing did not meet specifications, were distributed. |
| Initiation date | Jan 27, 2017 |
| Report date | Apr 5, 2017 |
| Termination date | Mar 29, 2017 |
| 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: