Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 75438 · Class II · Belle Bonfils Memorial Blood Center
Key facts
| Event ID | 75438 |
|---|---|
| Recall numbers | B-0092-2017, B-0093-2017 |
| Recalling firm | Belle Bonfils Memorial Blood Center |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob disease (vCJD), were distributed, Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob disease (vCJD), were distributed. |
| Initiation date | Aug 29, 2016 |
| Report date | Nov 9, 2016 |
| Termination date | Nov 1, 2016 |
| City | Denver |
| State | CO |
| Country | United States |
| FEI number | 3000210247 |
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: