Drug recall
PF24 Plasma
FDA recall event 95869 · Class III · Gulf Coast Regional Blood Center
Key facts
| Event ID | 95869 |
|---|---|
| Recall numbers | B-0120-2025 |
| Recalling firm | Gulf Coast Regional Blood Center |
| Product type | Biologics |
| Products | PF24 Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | PF24 Plasma product, for which a visual inspection was not performed or documented, was distributed. |
| Initiation date | Oct 10, 2024 |
| Report date | Dec 18, 2024 |
| Termination date | Dec 9, 2024 |
| City | Houston |
| State | TX |
| Country | United States |
| FEI number | 3002133806 |
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: