|
Model Number 6143.1001 |
Device Problem
Malposition of Device (2616)
|
Patient Problem
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
|
Event Date 10/23/2020 |
Event Type
Injury
|
Manufacturer Narrative
|
Investigation confirmed that there was no system malfunction found.The root cause was user technique.
|
|
Event Description
|
It was reported that the patient experienced foot drop post-operatively due to screws that were not placed to plan.The misplaced screws were removed and replaced.
|
|
Search Alerts/Recalls
|
|
|