Related manufacturing reference number: 2017865-2023-18408, related manufacturing reference number: 2017865-2023-18409, related manufacturing reference number: 2017865-2023-18412.It was reported that the patient presented with a fever and an infection.There was no allegation from a healthcare professional that the infection was caused or contributed to by the biventricular implantable cardioverter defibrillator (icd) system.An echocardiogram was performed and found that the right ventricular lead had vegetation.The icd, right ventricular, right atrial, and left ventricular leads were explanted and replaced with a leadless pacemaker.The patient was recovering post procedure.
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