Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 84200 · Class III · We Are Blood
Key facts
| Event ID | 84200 |
|---|---|
| Recall numbers | B-0159-2020 |
| Recalling firm | We Are Blood |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood products, which did not meet the acceptable product specifications, were distributed. |
| Initiation date | Sep 19, 2019 |
| Report date | Dec 18, 2019 |
| Termination date | Dec 6, 2019 |
| City | Austin |
| State | TX |
| Country | United States |
| FEI number | 1671794 |
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: