Drug recall
Source Plasma
FDA recall event 30956 · Class II · Bio-Blood Components, Inc.
Key facts
| Event ID | 30956 |
|---|---|
| Recall numbers | B-0692-5 |
| Recalling firm | Bio-Blood Components, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product tested negative for viral markers but was collected from an ineligible donor due to a risk factor for increased incidence of infection with human immunodeficiency virus (HIV). |
| Initiation date | Oct 15, 2004 |
| Termination date | Feb 22, 2005 |
| City | Hammond |
| Country | United States |
| FEI number | 1832147 |
At a glance
- 1–9 Products in this recall
- 1–9 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