Catalog Number 0210114100 |
Device Problem
Disassembly (1168)
|
Patient Problem
No Consequences Or Impact To Patient (2199)
|
Event Date 03/24/2014 |
Event Type
malfunction
|
Event Description
|
It was reported that the interpulse handpiece with coaxial high flow tip was being used in a procedure when the tip fell off and into the surgical site.The tip was removed by hand by the physician, and the procedure was completed successfully with the use of a back up device.There were no patient or user injuries, and no adverse consequences.
|
|
Manufacturer Narrative
|
A follow up report will be filed after the device is received and the quality investigation has been completed.Device not yet received by manufacturer.
|
|
Manufacturer Narrative
|
The device was not available to the manufacturer for evaluation, therefore, the reported event was unable to be confirmed.Not received for evaluation.
|
|
Event Description
|
It was reported that the interpulse handpiece with coaxial high flow tip was being used in a procedure when the tip fell off and into the surgical site.The tip was removed by hand by the physician, and the procedure was completed successfully with the use of a back up device.There were no patient or user injuries, and no adverse consequences.
|
|
Search Alerts/Recalls
|