Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 82543 · Class II · New York Blood Center, Inc.
Key facts
| Event ID | 82543 |
|---|---|
| Recall numbers | B-0472-2019, B-0473-2019, B-0474-2019 |
| Recalling firm | New York Blood Center, Inc. |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, PF24 Plasma, Red Blood Cells, Leukocytes Reduced |
| 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 | Mar 19, 2019 |
| Report date | Apr 17, 2019 |
| Termination date | Apr 5, 2019 |
| City | Westbury |
| State | NY |
| Country | United States |
| FEI number | 2470902 |
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: