Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 94097 · Class II · Coastal Bend Blood Center
Key facts
| Event ID | 94097 |
|---|---|
| Recall numbers | B-0194-2024 |
| Recalling firm | Coastal Bend Blood Center |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Apheresis Platelet products, collected from a donor whose suitability to donate was not adequately determined, were distributed. |
| Initiation date | Jan 15, 2024 |
| Report date | Mar 20, 2024 |
| Termination date | Mar 12, 2024 |
| City | Corpus Christi |
| State | TX |
| Country | United States |
| FEI number | 1671283 |
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: