Drug recall
Platelets Pheresis Leukocytes Reduced
FDA recall event 42800 · Class II · American National Red Cross (The)
Key facts
| Event ID | 42800 |
|---|---|
| Recall numbers | B-0361-13 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Platelets Pheresis Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, with unacceptable, undocumented or incomplete product QC and platelet counts were distributed. |
| Initiation date | Jul 26, 2006 |
| Report date | Dec 12, 2012 |
| Termination date | Dec 3, 2012 |
| City | Omaha |
| State | NE |
| Country | United States |
| FEI number | 1973037 |
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 · Source date: