Device Problems
Pocket Stimulation (1463); Device Dislodged or Dislocated (2923)
Patient Problem
No Consequences Or Impact To Patient (2199)
Event Date 04/09/2014
Event Type
Injury
Event Description
Boston scientific received information that this lead exhibited phrenic nerve stimulation and was not put in the ideal location.In addition, this lead then dislodged a day after the implant procedure.No additional adverse patient effects were reported.
Manufacturer Narrative
As no further information concerning this report is expected, our investigation is complete.This investigation will be updated should further information be provided.