Catalog Number 320-42-03 |
Device Problem
Device Operates Differently Than Expected (2913)
|
Patient Problem
Complaint, Ill-Defined (2331)
|
Event Date 11/09/2016 |
Event Type
Injury
|
Manufacturer Narrative
|
The contribution of the devices to the experience reported could not be determined as the devices were not returned for evaluation.Additionally, device specific information was not provided, precluding a review of the device history record.
|
|
Event Description
|
Patient presented with dislocation.The case report form indicates the event is unlikely related to devices and definitely related to the procedure.This event report was received through clinical data collection activities.
|
|
Manufacturer Narrative
|
The contribution of the devices to the experience reported could not be determined as the devices were not returned for evaluation.Additionally, device specific information was not provided, precluding a review of the device history record.
|
|
Event Description
|
Index surgery: (b)(6) 2014.Revision of right shoulder components due to dislocation.The case report form indicates the event is unlikely related to devices and definitely related to the procedure.This event report was received through clinical data collection activities.
|
|
Search Alerts/Recalls
|