Drug recall
Recovered Plasma 2 units 032GE56561, 032GE58023
FDA recall event 29743 · Class II · American National Red Cross (The)
Key facts
| Event ID | 29743 |
|---|---|
| Recall numbers | B-0125-7, B-0126-7 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Recovered Plasma 2 units 032GE56561, 032GE58023, Red Blood Cells, Leukocytes Reduced (2 units) 032GE56561, 032GE58023 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which tested negative for hepatitis, but were collected from an ineligible donor due to a subsequent disclosure of previous hepatitis testing, were distributed. |
| Initiation date | Jun 17, 2004 |
| Termination date | Nov 3, 2006 |
| City | Madison |
| Country | United States |
| FEI number | 2173028 |
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