Model Number 5100060001 |
Device Problem
Failure to Auto Stop (2938)
|
Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 07/07/2021 |
Event Type
malfunction
|
Manufacturer Narrative
|
A follow up report will be filed once the quality investigation is complete.Device discarded by customer.
|
|
Event Description
|
It was reported that during a cranial procedure, the perforator bit did not work.It was also reported that there was no adverse consequences as a result of this event.It was further reported that there was no surgical delay and the procedure was completed successfully.
|
|
Manufacturer Narrative
|
H6: the quality investigation is complete.H3 other text: device discarded by customer.
|
|
Event Description
|
It was reported that during a cranial procedure, the perforator bit did not work.It was also reported that there was no adverse consequences as a result of this event.It was further reported that there was no surgical delay and the procedure was completed successfully.
|
|
Search Alerts/Recalls
|