Drug recall
Source Plasma
FDA recall event 35218 · Class III · Stillwater Plasma Center, LLC
Key facts
| Event ID | 35218 |
|---|---|
| Recall numbers | B-0533-6 |
| Recalling firm | Stillwater Plasma Center, LLC |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma, which had not been tested for HIV NAT, was distributed. |
| Initiation date | Jun 11, 2004 |
| Termination date | Aug 11, 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