Drug recall
Source Plasma
FDA recall event 34926 · Class III · DCI Biologicals Wilmington, Inc.
Key facts
| Event ID | 34926 |
|---|---|
| Recall numbers | B-1220-6 |
| Recalling firm | DCI Biologicals Wilmington, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were untested for viral markers by the nucleic acleic acid test (NAT) method, were distributed. |
| Initiation date | Sep 22, 2005 |
| Termination date | Jun 8, 2006 |
| City | Wilmington |
| Country | United States |
| FEI number | 3003917693 |
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