Drug recall
Recovered Plasma
FDA recall event 32300 · Class II · Inland Northwest Blood Center
Key facts
| Event ID | 32300 |
|---|---|
| Recall numbers | B-1854-5 |
| Recalling firm | Inland Northwest Blood Center |
| Product type | Biologics |
| Products | Recovered Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, 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 | Mar 10, 2004 |
| Termination date | Aug 26, 2005 |
| City | Spokane |
| Country | United States |
| FEI number | 3071345 |
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