Related manufacturer reference number:2017865-2024-02081.Related manufacturer reference number:2017865-2024-02082.Related manufacturer reference number:2017865-2024-02083.It was reported that the patient presented in the clinic with an infection at the implanted device pocket site.It was also noted that the implantable cardioverter-defibrillator was visible from the opened incision site of the implanted device pocket.The implantable cardioverter defibrillator, right ventricular lead, right atrial lead were explanted and replaced with new system.There were no patient consequences reported.
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