Drug recall
Source Plasma
FDA recall event 51461 · Class III · Talecris Plasma Resources, Inc.
Key facts
| Event ID | 51461 |
|---|---|
| Recall numbers | B-0912-13 |
| Recalling firm | Talecris Plasma Resources, Inc. |
| 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 was previously deferred for unsuitable lab test results, were distributed. |
| Initiation date | Jan 29, 2009 |
| Report date | Feb 20, 2013 |
| Termination date | Feb 12, 2013 |
| City | Colorado Springs |
| State | CO |
| Country | United States |
| FEI number | 1718889 |
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 · Source date: