Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 82110 · Class II, Class III · OneBlood, Inc.
Key facts
| Event ID | 82110 |
|---|---|
| Recall numbers | B-0444-2019, B-0445-2019, B-0446-2019, B-0447-2019, B-0448-2019 |
| Recalling firm | OneBlood, Inc. |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, PF24 Plasma, Pooled Cryoprecipitated AHF, Red Blood Cells, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from an ineligible donor, were distributed. |
| Initiation date | Dec 18, 2018 |
| Report date | Apr 3, 2019 |
| Termination date | Mar 22, 2019 |
| City | St Petersburg |
| State | FL |
| Country | United States |
| FEI number | 1070196 |
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: