Drug recall
Source Plasma
FDA recall event 37092 · Class III · Knoxville Plasma Corp
Key facts
| Event ID | 37092 |
|---|---|
| Recall numbers | B-0716-7 |
| Recalling firm | Knoxville Plasma Corp |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who did not have a complete medical history interview, were distributed. |
| Initiation date | Aug 9, 2005 |
| Termination date | Feb 9, 2007 |
| City | Knoxville |
| Country | United States |
| FEI number | 1045035 |
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