Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 31983 · Class II · American Red Cross Blood Services HOA Region
Key facts
| Event ID | 31983 |
|---|---|
| Recall numbers | B-1327-5, B-1328-5 |
| Recalling firm | American Red Cross Blood Services HOA 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 | Blood products, collected in an apheresis collection kit that had exceeded the acceptable time period for use, were distributed. |
| Initiation date | Feb 21, 2005 |
| Termination date | Jun 3, 2005 |
| City | Peoria |
| Country | United States |
| FEI number | 1473043 |
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