Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 76563 · Class II · OneBlood, Inc.
Key facts
| Event ID | 76563 |
|---|---|
| Recall numbers | B-0407-2017 |
| Recalling firm | OneBlood, Inc. |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products collected from a donor for whom deferral screening was incorrectly performed, where distributed. |
| Initiation date | Jan 20, 2017 |
| Report date | Mar 22, 2017 |
| Termination date | Mar 15, 2017 |
| City | Orlando |
| State | FL |
| Country | United States |
| FEI number | 1072425 |
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: