Drug recall
PF24 Plasma
FDA recall event 78749 · Class II · The American National Red Cross - Southern Region
Key facts
| Event ID | 78749 |
|---|---|
| Recall numbers | B-0233-2018 |
| Recalling firm | The American National Red Cross - Southern Region |
| Product type | Biologics |
| Products | PF24 Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, in which donor suitability was not adequately determined, was distributed. |
| Initiation date | Oct 13, 2017 |
| Report date | Jan 24, 2018 |
| Termination date | Jan 12, 2018 |
| City | Douglasville |
| State | GA |
| Country | United States |
| FEI number | 1073000 |
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: