Drug recall
Source Plasma
FDA recall event 35980 · Class II · BioLife Plasma Services LP
Key facts
| Event ID | 35980 |
|---|---|
| Recall numbers | B-0167-7 |
| Recalling firm | BioLife Plasma Services LP |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who was at increased risk for new variant Creutzfeldt-Jakob Disease (nvCJD), were distributed. |
| Initiation date | Apr 5, 2004 |
| Termination date | Nov 14, 2006 |
| City | Deerfield |
| 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