Related manufacturer reference number: 2017865-2020-23387.It was reported that the patient presented for an implant procedure.During the procedure, the physician was having difficulty implanting the left ventricular (lv) lead due to the poor angle of the target vessel.The inner cavity of the lead entered the blood, and the guidewire could not be inserted to the tip.The lead was removed and replaced.The 2nd lead was unable to enter the target blood vessel after more than a hour of trying.The 2nd lead was also removed and replaced.The patient was stable.
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