Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 75506 · Class II · Aurora Area Blood Bank Dba Heartland Blood Centers
Key facts
| Event ID | 75506 |
|---|---|
| Recall numbers | B-0125-2017 |
| Recalling firm | Aurora Area Blood Bank Dba Heartland Blood Centers |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | RBC product, for which quality control and distribution of product did not meet specifications, was distributed. |
| Initiation date | Sep 13, 2016 |
| Report date | Nov 9, 2016 |
| Termination date | Nov 3, 2016 |
| City | Aurora |
| State | IL |
| Country | United States |
| FEI number | 1470274 |
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: