Drug recall
Recovered Plasma
FDA recall event 26078 · Class II, Class III · Carter BloodCare
Key facts
| Event ID | 26078 |
|---|---|
| Recall numbers | B-1307-3, B-1308-3 |
| Recalling firm | Carter BloodCare |
| Product type | Biologics |
| Products | Recovered Plasma, Red Blood Cells |
| Classification | Class II, Class III |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who affirmatively answered a medical history question related to increase risk of infection with the human immunodeficiency virus (HIV), were distributed. |
| Initiation date | Jul 5, 2001 |
| City | Bedford |
| Country | United States |
| FEI number | 3002603147 |
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