Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 76876 · Class II · LifeShare Community Blood Services
Key facts
| Event ID | 76876 |
|---|---|
| Recall numbers | B-0496-2017 |
| Recalling firm | LifeShare Community Blood Services |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis product, in which quality control for WBC count was not performed within 48 hour of collection, was distributed. |
| Initiation date | Mar 8, 2017 |
| Report date | Apr 26, 2017 |
| Termination date | Apr 19, 2017 |
| City | Elyria |
| State | OH |
| Country | United States |
| FEI number | 1523639 |
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: