Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 31343 · Class II · American Red Cross Blood Services Tennessee Valley Region
Key facts
| Event ID | 31343 |
|---|---|
| Recall numbers | B-0964-5, B-0965-5 |
| Recalling firm | American Red Cross Blood Services Tennessee Valley Region |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced, Platelets Pheresis, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Platelet Pheresis products, lacking monthly quality control testing, were distributed. |
| Initiation date | Dec 24, 2003 |
| Termination date | Apr 22, 2005 |
| City | Nashville |
| Country | United States |
| FEI number | 1073006 |
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