Drug recall
Source Plasma
FDA recall event 30264 · Class II · Zlb Bioplasma, Inc.
Key facts
| Event ID | 30264 |
|---|---|
| Recall numbers | B-1105-5 |
| Recalling firm | Zlb Bioplasma, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Completed |
| 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 23, 2002 |
| City | Salt Lake City |
| Country | United States |
| FEI number | 1721835 |
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