Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 50296 · Class II, Class III · American National Red Cross (The)
Key facts
| Event ID | 50296 |
|---|---|
| Recall numbers | B-0722-13, B-0723-13 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Red Blood Cells Leukocytes Reduced |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed. |
| Initiation date | Oct 17, 2008 |
| Report date | Jan 16, 2013 |
| Termination date | Jan 4, 2013 |
| 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: