Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated
FDA recall event 80798 · Class II · New York Blood Center, Inc.
Key facts
| Event ID | 80798 |
|---|---|
| Recall numbers | B-0742-2018, B-0743-2018 |
| Recalling firm | New York Blood Center, Inc. |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated, Pooled Cryoprecipitated AHF |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor for whom donor suitability was not adequately determined, were distributed. |
| Initiation date | Jul 6, 2018 |
| Report date | Aug 29, 2018 |
| Termination date | Aug 22, 2018 |
| City | New York |
| State | NY |
| Country | United States |
| FEI number | 2476837 |
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: