Drug recall
Source Plasma
FDA recall event 45721 · Class II · BioLife Plasma Services L.P.
Key facts
| Event ID | 45721 |
|---|---|
| Recall numbers | B-0347-13 |
| Recalling firm | BioLife Plasma Services L.P. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, identified as unsuitable due to a donor screening deviation, was distributed. |
| Initiation date | Sep 25, 2007 |
| Report date | Nov 21, 2012 |
| Termination date | Nov 14, 2012 |
| City | Springfield |
| State | MO |
| Country | United States |
| FEI number | 1978019 |
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: