Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 78557 · Class II, Class III · New York Blood Center, Inc.
Key facts
| Event ID | 78557 |
|---|---|
| Recall numbers | B-0133-2018, B-0134-2018, B-0135-2018, B-0136-2018 |
| Recalling firm | New York Blood Center, Inc. |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, PF24 Plasma, Red Blood Cells, Leukocytes Reduced, Red Blood Cells, Leukocytes Reduced, Irradiated |
| Classification | Class II, Class III |
| 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 | Oct 4, 2017 |
| Report date | Dec 6, 2017 |
| Termination date | Nov 29, 2017 |
| City | New Brunswick |
| State | NJ |
| Country | United States |
| FEI number | 2276020 |
At a glance
- 1–9 Products in this recall
- None 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: