Drug recall
Platelets
FDA recall event 31289 · Class II · Central Blood Bank
Key facts
| Event ID | 31289 |
|---|---|
| Recall numbers | B-1834-6, B-1835-6, B-1836-6 |
| Recalling firm | Central Blood Bank |
| Product type | Biologics |
| Products | Platelets, Recovered Plasma, Red Blood Cells |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which tested negative for hepatitis, but were collected from a donor who was subsequently determined to have been deferred for testing positive for Hepatitis C, were distributed. |
| Initiation date | Dec 28, 2004 |
| Termination date | Sep 22, 2006 |
| City | Pittsburgh |
| Country | United States |
| FEI number | 2571073 |
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