Related manufacturer reference 9680001-2016-00020, 9680001-2016-00022, 3005188751-2016-00009, 3005334138-2016-00010, 2030404-2016-00007, 3005188751-2016-00010.Following an atrial fibrillation ablation procedure, a cerebrovascular accident occurred.During the procedure a rise in impedance occurred and the ablation catheter was exchanged for another of the same model to complete the procedure.Following the procedure, the patient experienced double vision and an mri was performed, which revealed a cerebrovascular accident.No intervention was required to treat the patient and the patient was stable with double vision and issues with equilibrium at the time of this report.The physician was uncertain as to the cause of the cerebrovascular accident.
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