Catalog Number UNK-ASR |
Device Problem
Device Dislodged or Dislocated (2923)
|
Patient Problems
Pain (1994); Discomfort (2330); Joint Dislocation (2374)
|
Event Date 06/12/2015 |
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.This complaint is the subject of litigation or a legal claim and currently complete product detail is not available at this time.A follow-up medwatch will be filed as appropriate.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
|
|
Event Description
|
On (b)(6) 2017.Litigation recieved.Litigation alleges pain, discomfort and dislocation.
|
|
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
|