Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 80935 · Class II · Mississippi Valley Reg Bld Ctr
Key facts
| Event ID | 80935 |
|---|---|
| Recall numbers | B-0010-2019 |
| Recalling firm | Mississippi Valley Reg Bld Ctr |
| 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 considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed. |
| Initiation date | Jul 23, 2018 |
| Report date | Oct 24, 2018 |
| Termination date | Oct 12, 2018 |
| City | Davenport |
| State | IA |
| Country | United States |
| FEI number | 1970356 |
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: