Drug recall
Platelets Pheresis Leukocytes Reduced
FDA recall event 61971 · Class II · LifeSource
Key facts
| Event ID | 61971 |
|---|---|
| Recall numbers | B-1725-12 |
| Recalling firm | LifeSource |
| Product type | Biologics |
| Products | Platelets Pheresis Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, labeled leukoreduced without the assurance that they met the criteria for leukoreduced products, were distributed. |
| Initiation date | Apr 9, 2012 |
| Report date | Jun 20, 2012 |
| Termination date | Jun 11, 2012 |
| City | Rosemont |
| State | IL |
| Country | United States |
| FEI number | 3008744215 |
At a glance
- 1–9 Products in this recall
- 1–9 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: