It was reported that during use of the device for a cardiopulmonary bypass (cpb) procedure, there were intermittent level sensor alarms with the yellow level sensor on the perfusion system.The issue occurred during the case repeatedly and the alarm message was not appearing on top of the screen.The device was not changed out, as they continued the case with the nuisance alarm and surgery was successful.There was no delay, no blood loss, nor adverse consequences to the patient.Per the clinical review on (b)(6) 2014: the system-1 (with level sensor) was used with the sorin synthesis oxygenator and venous reservoir.The reservoir is round and they have had coupling issues in the past.During cpb, they had a couple incidents of "level not attached" messages where the sensor lost adequate coupling to the reservoir.There was an audible tone, but no message was posted on the main screen of the central control monitor (ccm).The "message" tab of the aux screen did post a message related to level.After the second alert, the ccp turned the level sensor off and she added more gel to the sensor face and re-attached to the sensor pad.There were no other issues with coupling problems the remainder of the procedure.The case was completed successfully, without delay and without associated blood loss.There was no harm observed.
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This complaint is related to mdr#: 1828100-2014-01139.Per field service rep (fsr), the issue occurred so fast that they could not determine if it was the yellow or the red sensor.The fsr could no duplicate the reported complaint but he found the contact surface of yellow sensor serial number (b)(4), was slightly concave and may not have been making good contact with the reservoir.The fsr downloaded the data logs and will submit to the manufacturer for further evaluation.
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