Drug recall
Platelet Pheresis, Leukocytes Reduced, Irradiated
FDA recall event 74267 · Class III · LifeServe Blood Center
Key facts
| Event ID | 74267 |
|---|---|
| Recall numbers | B-0618-16 |
| Recalling firm | LifeServe Blood Center |
| Product type | Biologics |
| Products | Platelet Pheresis, Leukocytes Reduced, Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Platelet, labeled with an incorrect volume, was distributed. |
| Initiation date | Apr 18, 2016 |
| Report date | Jul 20, 2016 |
| Termination date | Jul 8, 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: