Drug recall
SmartSite Extension Set, Model No. 20029E, intravascular administration set.
FDA recall event 67774 · Class II · CareFusion 303, Inc.
Key facts
| Event ID | 67774 |
|---|---|
| Recall numbers | Z-1459-2014 |
| Recalling firm | CareFusion 303, Inc. |
| Product type | Devices |
| Products | SmartSite Extension Set, Model No. 20029E, intravascular administration set. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port. |
| Initiation date | Mar 19, 2014 |
| Report date | Apr 23, 2014 |
| Termination date | Jun 6, 2015 |
| City | San Diego |
| State | CA |
| Country | United States |
| FEI number | 2016493 |
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: