Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 83122 · Class III · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 83122 |
|---|---|
| Recall numbers | B-0719-2019 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman Center |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis Red Blood Cell products, not meeting product specifications, were distributed. |
| Initiation date | Mar 4, 2019 |
| Report date | Jul 10, 2019 |
| Termination date | Jun 28, 2019 |
| 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: