| Model Number |
TPS121111102 |
| Health Effect - Clinical Code |
Insufficient Information (4580)
|
| Date of Event |
10/01/2020
|
|
Type of Reportable Event
|
Serious Injury
|
|
Additional Manufacturer Narrative
|
|
It was reported that the patient has laxity and requires revision surgery is planned to exchange the poly insert.Review of the device history record indicates that the device was manufactured to specification.
|
| |
|
Event or Problem Description
|
|
It was reported that the patient has laxity and requires revision surgery is planned to exchange the poly insert.
|
| |
|
Search Alerts/Recalls
|