Drug recall
Platelets Leukocytes Reduced, Irradiated
FDA recall event 31524 · Class III · Carter BloodCare
Key facts
| Event ID | 31524 |
|---|---|
| Recall numbers | B-1430-5, B-1431-5, B-1432-5 |
| Recalling firm | Carter BloodCare |
| Product type | Biologics |
| Products | Platelets Leukocytes Reduced, Irradiated, Platelets Pheresis, Leukocytes Reduced, Platelets Pheresis, Leukocytes Reduced, Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, with incomplete bacterial detection testing performed , were distributed., Blood products, with incomplete bacterial detection testing performed, were distributed. |
| Initiation date | Apr 8, 2004 |
| Termination date | Jul 6, 2005 |
| City | Bedford |
| Country | United States |
| FEI number | 3002603147 |
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