Drug recall
Platelets Pheresis Leukocytes Reduced
FDA recall event 46543 · Class II · American Red Cross Blood Services
Key facts
| Event ID | 46543 |
|---|---|
| Recall numbers | B-0570-13 |
| Recalling firm | American Red Cross Blood Services |
| Product type | Biologics |
| Products | Platelets Pheresis Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, manufactured from an apheresis unit with platelet yield that did not meet the criteria for a divided unit, were distributed. |
| Initiation date | Nov 14, 2007 |
| Report date | Jan 2, 2013 |
| Termination date | Dec 27, 2012 |
| City | Saint Louis |
| State | MO |
| Country | United States |
| FEI number | 1973035 |
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: