Drug recall
Source Plasma
FDA recall event 35225 · Class II · Stillwater Plasma Center, LLC
Key facts
| Event ID | 35225 |
|---|---|
| Recall numbers | B-1451-6 |
| Recalling firm | Stillwater Plasma Center, LLC |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were untested fro viral markers by the nucleic acid test (NAT) method, were distributed. |
| Initiation date | Jun 11, 2004 |
| Termination date | Sep 22, 2006 |
| City | Stillwater |
| Country | United States |
| FEI number | 1643932 |
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