Catalog Number ES-04522 |
Device Problems
Fluid/Blood Leak (1250); Material Perforation (2205)
|
Patient Problem
No Consequences Or Impact To Patient (2199)
|
Event Date 01/16/2017 |
Event Type
malfunction
|
Manufacturer Narrative
|
(b)(4).The results of the investigation are pending at the time of this report.
|
|
Event Description
|
The customer reports that when the catheter was placed, there was some evidence of fluid leaking.When removing the catheter, it appeared to be perforated.No patient injury reported.No intervention required.
|
|
Manufacturer Narrative
|
(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.A device history record review could not be performed as no lot number was provided by the customer.Without the device to evaluate, the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.
|
|
Event Description
|
The customer reports that when the catheter was placed, there was some evidence of fluid leaking.When removing the catheter, it appeared to be perforated.No patient injury reported.No intervention required.
|
|
Search Alerts/Recalls
|