Drug recall
Source Plasma
FDA recall event 26882 · Class II · DCI Biologicals Carbondale, LLC
Key facts
| Event ID | 26882 |
|---|---|
| Recall numbers | B-1694-3 |
| Recalling firm | DCI Biologicals Carbondale, LLC |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected in a manner that compromises the sterility of the collection system, was distributed. |
| Initiation date | Jun 2, 2003 |
| City | Carbondale |
| Country | United States |
| FEI number | 3001451631 |
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