Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 76578 · Class II · Delta Blood Bank
Key facts
| Event ID | 76578 |
|---|---|
| Recall numbers | B-0474-2017, B-0475-2017, B-0476-2017 |
| Recalling firm | Delta Blood Bank |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Apheresis Platelets, Leukocytes Reduced, Irradiated, Washed Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, tested with expired reagents, were distributed. |
| Initiation date | Jan 11, 2017 |
| Report date | Apr 5, 2017 |
| Termination date | Mar 30, 2017 |
| City | Stockton |
| State | CA |
| Country | United States |
| FEI number | 2970116 |
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: