Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 48508 · Class II · Blood Systems, Inc.
Key facts
| Event ID | 48508 |
|---|---|
| Recall numbers | B-2461-13 |
| Recalling firm | Blood Systems, Inc. |
| 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 was not tested to verify the White Blood Cell count, was distributed. |
| Initiation date | Apr 11, 2008 |
| Report date | Sep 11, 2013 |
| Termination date | Sep 5, 2013 |
| City | Scottsdale |
| State | AZ |
| Country | United States |
| FEI number | 2071464 |
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: