Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 31465 · Class III · Carter BloodCare
Key facts
| Event ID | 31465 |
|---|---|
| Recall numbers | B-1053-5, B-1054-5, B-1055-5, B-1056-5, B-1057-5, B-1058-5, B-1059-5 |
| Recalling firm | Carter BloodCare |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced, Platelets Pheresis, Leukocytes Reduced, Irradiated, Red Blood Cells, Leukocytes Reduced, Red Blood Cells, Leukocytes Reduced Irradiated, Red Blood Cells, Leukocytes Reduced Washed and 2 more |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were labeled leukoreduced, but ahd an unacceptable white blood cell count, were distributed. |
| Initiation date | Oct 10, 2003 |
| Termination date | May 19, 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