Drug recall
Red Blood Cells Leukocytes Reduced
FDA recall event 52884 · Class II · American National Red Cross (The)
Key facts
| Event ID | 52884 |
|---|---|
| Recall numbers | B-2362-13 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Red Blood Cells Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were collected in a collection system that may have a potential defect which could compromise the sterility of the closed system, were distributed. |
| Initiation date | Jun 26, 2009 |
| Report date | Aug 21, 2013 |
| Termination date | Aug 9, 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: