Drug recall
Red Blood Cells, Leukocytes Reduced, Irradiated
FDA recall event 73929 · Class III · The Blood Alliance, Inc.
Key facts
| Event ID | 73929 |
|---|---|
| Recall numbers | B-0522-16 |
| Recalling firm | The Blood Alliance, Inc. |
| Product type | Biologics |
| Products | Red Blood Cells, Leukocytes Reduced, Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, in which quality control and distribution of products did not meet specifications, were distributed. |
| Initiation date | Mar 25, 2016 |
| Report date | Jun 1, 2016 |
| Termination date | May 24, 2016 |
| 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: