Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 71660 · Class II · Inland Northwest Blood Center
Key facts
| Event ID | 71660 |
|---|---|
| Recall numbers | B-0826-15 |
| Recalling firm | Inland Northwest Blood Center |
| Product type | Biologics |
| Products | Red Blood Cells (Apheresis) Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, labeled as leukoreduced, but exceeded the acceptable White Blood Cell count (WBC), was distributed. |
| Initiation date | May 28, 2015 |
| Report date | Aug 12, 2015 |
| Termination date | Aug 4, 2015 |
| 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: