Drug recall
Recovered Plasma
FDA recall event 37861 · Class II, Class III · American Natl Red Cross Mid At
Key facts
| Event ID | 37861 |
|---|---|
| Recall numbers | B-1388-07, B-1389-07 |
| Recalling firm | American Natl Red Cross Mid At |
| Product type | Biologics |
| Products | Recovered Plasma, Red Blood Cells |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was collected from a donor in which donor suitability was not adequately determined, was distributed. |
| Initiation date | Jun 30, 2006 |
| Termination date | Sep 21, 2007 |
| City | Norfolk |
| State | VA |
| Country | United States |
| FEI number | 1173024 |
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