Related manufacturer reference number: 2017865-2022-50852, 2017865-2022-50854, 2017865-2022-50855.It was reported that the patient presented with infection and skin erosion at device pocket site during follow-up in clinic.The implanted device pocket was noted to be red.The physician explanted the system ¿ implantable cardioverter defibrillator, atrial lead, right ventricular lead and left ventricular lead.The system was replaced with implantable cardioverter defibrillator, atrial lead, right ventricular lead and left ventricular lead.The patient was in stable condition.
|