Drug recall
Apheresis Plasma Frozen withing 24 hours After Phlebotomy
FDA recall event 73399 · Class II, Class III · Mississippi Valley Regional Blood Center
Key facts
| Event ID | 73399 |
|---|---|
| Recall numbers | B-0325-16, B-0326-16, B-0327-16, B-0328-16, B-0329-16, B-0330-16, B-0331-16, B-0332-16, B-0333-16, B-0334-16, B-0335-16, B-0336-16 and 8 more |
| Recalling firm | Mississippi Valley Regional Blood Center |
| Product type | Biologics |
| Products | Apheresis Plasma Frozen withing 24 hours After Phlebotomy, Apheresis Plasma Frozen withing 24 Hours After Phlebotomy, Apheresis Platelets, Leukocytes Reduced, Apheresis Red Blood Cells, Leukocytes Reduced, Blood and Blood Products for Reprocessing and 9 more |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, incorrectly tested for antibodies to HCV (anti-HCV), were distributed. |
| Initiation date | Nov 20, 2015 |
| Report date | Mar 16, 2016 |
| Termination date | Aug 11, 2017 |
| City | Davenport |
| State | IA |
| Country | United States |
| FEI number | 1970356 |
At a glance
- 10–99 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: