Catalog Number UNK-HIP |
Device Problem
Malposition of Device (2616)
|
Patient Problem
No Information (3190)
|
Event Date 05/17/2017 |
Event Type
Injury
|
Manufacturer Narrative
|
This complaint is still under investigation.Depuy will notify the fda of the results of this investigation once it has been completed.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
|
|
Event Description
|
Patient was revised to address dislocation of the bipolar system.It was also indicated that the surgeon wanted to change the version of the stem.Update 5/17/2017: reviewed der and assessed reportability.The previously added unknown liner was removed and voided, as it is not a part of and unnecessary with a bipolar construct.
|
|
Manufacturer Narrative
|
No device associated with this report was received for examination.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
|
|
Search Alerts/Recalls
|