Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 72109 · Class II, Class III · American Natl. Red Cross-Greater Chesapeake & Potomac Region
Key facts
| Event ID | 72109 |
|---|---|
| Recall numbers | B-0049-16, B-0050-16, B-0051-16 |
| Recalling firm | American Natl. Red Cross-Greater Chesapeake & Potomac Region |
| Product type | Biologics |
| Products | Red Blood Cells (Apheresis) Leukocytes Reduced, Red Blood Cells Leukocytes Reduced |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, for which testing was not performed according to manufacturer's instructions, were distributed. |
| Initiation date | Jul 8, 2015 |
| Report date | Oct 21, 2015 |
| Termination date | Oct 15, 2015 |
| City | Baltimore |
| State | MD |
| Country | United States |
| FEI number | 1173011 |
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: