Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 68057 · Class II · The Blood Alliance, Inc.
Key facts
| Event ID | 68057 |
|---|---|
| Recall numbers | B-0650-14, B-0651-14 |
| Recalling firm | The Blood Alliance, Inc. |
| Product type | Biologics |
| Products | Red Blood Cells (Apheresis) Leukocytes Reduced, Red Blood Cells (Apheresis) Leukocytes Reduced Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, not prepared in accordance with specifications and which failed to meet product specifications, were distributed. |
| Initiation date | Mar 3, 2014 |
| Report date | Jun 18, 2014 |
| Termination date | Jun 11, 2014 |
| City | Jacksonville |
| State | FL |
| Country | United States |
| FEI number | 1071473 |
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: