Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 87921 · Class II · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 87921 |
|---|---|
| Recall numbers | B-0457-2021 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman Center |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Apheresis Red Blood Cell products, for which quality control for residual white blood cell count testing was not performed, were distributed. |
| Initiation date | Mar 30, 2021 |
| Report date | Jun 16, 2021 |
| Termination date | Jun 7, 2021 |
| City | Oklahoma City |
| State | OK |
| Country | United States |
| FEI number | 1626009 |
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: