Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 35662 · Class III · Central Indiana Regional Blood Center, Inc
Key facts
| Event ID | 35662 |
|---|---|
| Recall numbers | B-1839-6 |
| Recalling firm | Central Indiana Regional Blood Center, Inc |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Platelets, which were possibly contaminated with Propionibacterium species, were distributed. |
| Initiation date | May 18, 2006 |
| Termination date | Sep 21, 2006 |
| City | Indianapolis |
| Country | United States |
| FEI number | 1873403 |
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