Drug recall
Recovered Plasma
FDA recall event 26473 · Class III · WE & Lela I Stewart Blood Center, Inc
Key facts
| Event ID | 26473 |
|---|---|
| Recall numbers | B-1404-3, B-1405-3 |
| Recalling firm | WE & Lela I Stewart Blood Center, Inc |
| Product type | Biologics |
| Products | Recovered Plasma, Red Blood Cells |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, that tested negative for antibodies to human immunodeficiency virus (anti-HIV), but were collected from a donor that previously tested repeatedly reactive for anti-HIV, were… |
| Initiation date | Feb 16, 2001 |
| City | Tyler |
| Country | United States |
| FEI number | 1672331 |
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