Drug recall
Plasma Frozen
FDA recall event 48234 · Class II · American National Red Cross (The)
Key facts
| Event ID | 48234 |
|---|---|
| Recall numbers | B-1650-13, B-1651-13, B-1652-13 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Plasma Frozen, Platelets Leukocytes Reduced, Red Blood Cells Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed. |
| Initiation date | Mar 25, 2008 |
| Report date | May 8, 2013 |
| Termination date | Apr 29, 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: