Related manufacturing reference: 3008452825-2019-00022, 3005334138-2019-00028, 3008452825-2019-00023, 3005334138-2019-00030, 2182269-2019-00007.Following an atrial fibrillation procedure, the patient expired.During the procedure, the septum felt hard (non-elastic), fibrotic and resistant due to a previous procedure.During post procedure hospitalization, a pericardial effusion was discovered which evolved into cardiac arrest during the night.Reanimation with cardiac massage was performed, however the effect of the cardiac arrest led to cerebral death eight days post procedure and the patient expired on (b)(6) 2019.There were no performance issues with any abbott devices.
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