Drug recall
Source Plasma
FDA recall event 42204 · Class III · BioLife Plasma Services L.P.
Key facts
| Event ID | 42204 |
|---|---|
| Recall numbers | B-1141-13 |
| Recalling firm | BioLife Plasma Services L.P. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor for whom donor suitability was not adequately determined, was distributed. |
| Initiation date | May 24, 2006 |
| Report date | Mar 13, 2013 |
| Termination date | Mar 7, 2013 |
| City | Coralville |
| State | IA |
| Country | United States |
| FEI number | 1937444 |
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: