Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 82358 · Class II · Mississippi Valley Reg Bld Ctr
Key facts
| Event ID | 82358 |
|---|---|
| Recall numbers | B-0462-2019 |
| Recalling firm | Mississippi Valley Reg Bld Ctr |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, incorrectly tested and labeled for a red cell antigen, were distributed. |
| Initiation date | Jan 23, 2019 |
| Report date | Apr 24, 2019 |
| Termination date | Apr 15, 2019 |
| City | Davenport |
| State | IA |
| Country | United States |
| FEI number | 1970356 |
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: