Drug recall
PF24 Plasma
FDA recall event 79357 · Class II · American Natl Red Cross Mid Atlantic Region
Key facts
| Event ID | 79357 |
|---|---|
| Recall numbers | B-0405-2018 |
| Recalling firm | American Natl Red Cross Mid Atlantic Region |
| Product type | Biologics |
| Products | PF24 Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Initiation date | Jan 27, 2018 |
| Report date | Mar 14, 2018 |
| Termination date | Mar 7, 2018 |
| City | Norfolk |
| State | VA |
| Country | United States |
| FEI number | 1173024 |
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: