Drug recall
Source Plasma
FDA recall event 75233 · Class III · DCI Biologicals Greenville, Inc
Key facts
| Event ID | 75233 |
|---|---|
| Recall numbers | B-0037-2017 |
| Recalling firm | DCI Biologicals Greenville, Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor in which donor suitability was not adequately determined, was distributed. |
| Initiation date | Jun 23, 2016 |
| Report date | Oct 26, 2016 |
| Termination date | Oct 18, 2016 |
| City | Greenville |
| State | NC |
| Country | United States |
| FEI number | 3003645334 |
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 · Source date: