Drug recall
Apheresis Platelets, Leukocytes Reduced, Irradiated
FDA recall event 73839 · Class II · LifeServe Blood Center
Key facts
| Event ID | 73839 |
|---|---|
| Recall numbers | B-0432-16 |
| Recalling firm | LifeServe Blood Center |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis Platelets, lacking proper quality control testing, were distributed. |
| Initiation date | Mar 15, 2016 |
| Report date | Apr 20, 2016 |
| Termination date | Apr 14, 2016 |
| 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: