Drug recall
PF24 Plasma
FDA recall event 80339 · Class II · HCSC Blood Center dba as Miller-Keystone Blood Center
Key facts
| Event ID | 80339 |
|---|---|
| Recall numbers | B-0640-2018, B-0641-2018 |
| Recalling firm | HCSC Blood Center dba as Miller-Keystone Blood Center |
| Product type | Biologics |
| Products | PF24 Plasma, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products collected from a donor for whom donor suitability was not adequately determined, were distributed. |
| Initiation date | May 22, 2018 |
| Report date | Jul 4, 2018 |
| Termination date | Jun 26, 2018 |
| City | Bethlehem |
| State | PA |
| Country | United States |
| FEI number | 2573135 |
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: