Drug recall
Source Plasma
FDA recall event 39808 · Class III · BioLife Plasma Services LP
Key facts
| Event ID | 39808 |
|---|---|
| Recall numbers | B-1054-08 |
| Recalling firm | BioLife Plasma Services LP |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were not quarantined after the donor provided information concerning a post-donation illness, were distributed. |
| Initiation date | Feb 11, 2005 |
| Termination date | Apr 1, 2008 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 3004414580 |
At a glance
- 1–9 Products in this recall
- 1–9 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