Drug recall
Platelet Pheresis, Leukoreduced
FDA recall event 29139 · Class II · American National Red Cross Great Lakes Region
Key facts
| Event ID | 29139 |
|---|---|
| Recall numbers | B-1578-4, B-1579-4 |
| Recalling firm | American National Red Cross Great Lakes Region |
| Product type | Biologics |
| Products | Platelet Pheresis, Leukoreduced, Platelet Pheresis, Leukoreduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood Products, which were collected in an apheresis collection kit that may have exceeded the acceptable time period for use, were distributed. |
| Initiation date | Apr 2, 2004 |
| Termination date | Jul 21, 2004 |
| City | Lansing |
| Country | United States |
| FEI number | 1873033 |
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