Drug recall
Platelets Leukocytes Reduced
FDA recall event 50623 · Class II · American National Red Cross (The)
Key facts
| Event ID | 50623 |
|---|---|
| Recall numbers | B-1627-13, B-1628-13 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Platelets Leukocytes Reduced, Red Blood Cells Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, in which routine testing interpreted or documented incorrectly, were distributed. |
| Initiation date | Oct 30, 2008 |
| Report date | May 22, 2013 |
| Termination date | May 10, 2013 |
| City | West Henrietta |
| State | NY |
| Country | United States |
| FEI number | 3002957282 |
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: