FDA Device recall Z-1459-2014
SmartSite Extension Set, Model No. 20029E, intravascular administration set
- FDA Device
- Class II
- terminated
- Published 2014-04-23
On 2014-04-23 the FDA classified a Class II recall of SmartSite Extension Set, Model No. 20029E, intravascular administration set by Carefusion 303, citing disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1459-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-19 |
| Published | 2014-04-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
SmartSite Extension Set, Model No. 20029E, intravascular administration set.
Reason
Disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port.
Identifiers
| code_info | Lot No. 13085791 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1459-2014%22
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