Drug recall
Source Plasma
FDA recall event 35344 · Class II · ZLB Bioplasma, Inc
Key facts
| Event ID | 35344 |
|---|---|
| Recall numbers | B-0164-7 |
| Recalling firm | ZLB Bioplasma, Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma, collected from a donor whose medical history screening did not include questioning regarding risk factors for Creutzfeldt-Jakob Disease (CJD) and variant Creutzfeldt-Jakob Disease… |
| Initiation date | Dec 19, 2002 |
| Termination date | Nov 14, 2006 |
| City | Duluth |
| Country | United States |
| FEI number | 2176201 |
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