Drug recall
Apheresis Platelets, Leukocytes Reduced, Irradiated
FDA recall event 75102 · Class II · Inland Northwest Blood Center
Key facts
| Event ID | 75102 |
|---|---|
| Recall numbers | B-0768-16 |
| Recalling firm | Inland Northwest 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 products, in which quality control for residual WBC count was not performed, were distributed. |
| Initiation date | Aug 26, 2016 |
| Report date | Sep 28, 2016 |
| Termination date | Sep 19, 2016 |
| City | Spokane |
| State | WA |
| Country | United States |
| FEI number | 3071345 |
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: