Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 82031 · Class II · OneBlood, Inc.
Key facts
| Event ID | 82031 |
|---|---|
| Recall numbers | B-0349-2019 |
| Recalling firm | OneBlood, Inc. |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which did not meet the acceptable product specifications for release, were distributed. |
| Initiation date | Nov 5, 2018 |
| Report date | Mar 13, 2019 |
| Termination date | Mar 4, 2019 |
| 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: