Drug recall
Source Plasma
FDA recall event 31695 · Class II · Zlb Bioplasma Services
Key facts
| Event ID | 31695 |
|---|---|
| Recall numbers | B-1100-5 |
| Recalling firm | Zlb Bioplasma Services |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor whose medical history screening did not include questioning regarding risk factors for Creutzfeldt-Jacob disease (vCJD), were distributed. |
| Initiation date | Dec 4, 2002 |
| City | Boca Raton |
| Country | United States |
| FEI number | 3003507515 |
At a glance
- 1–9 Products in this recall
- None 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