Catalog Number PS-01652 |
Device Problems
Obstruction of Flow (2423); Improper Flow or Infusion (2954)
|
Patient Problem
No Consequences Or Impact To Patient (2199)
|
Event Date 10/22/2019 |
Event Type
malfunction
|
Manufacturer Narrative
|
(b)(4).Dhr conducted and no relevant findings were noted.
|
|
Event Description
|
The customer reports that the catheter is occluded and there is a return of liquid by the alternate road (line).Another device was used.
|
|
Manufacturer Narrative
|
Qn# (b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.A device history record review was performed and no relevant findings were identified.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.If the sample becomes available at a later date a follow up report will be submitted with investigation results.
|
|
Event Description
|
The customer reports that the catheter is occluded and there is a return of liquid by the alternate road (line).Another device was used.
|
|
Search Alerts/Recalls
|