Related manufacturer reference number: 2017865-2021-40055.Related manufacturer reference number: 2017865-2021-40065.Related manufacturer reference number: 2017865-2021-40068.It was reported that the patient experienced fever due to an infection.There is no allegation that the abbott devices or any procedure involving the abbott devices, caused or contributed to the infection.The implantable cardioverter defibrillator, right ventricular lead, left ventricular lead, and atrial lead was explanted.There were no patient consequences.
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