MAUDE Adverse Event Report: EDWARDS LIFESCIENCES CLEARSIGHT MODULE

Model Number	HEMCSM10
Medical Device Problem Code	Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/20/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device has been requested to be returned for evaluation.It has not arrived yet.Once the evaluation has been completed, the evaluation results will be submitted in a supplemental submission.The device history record review is pending.Once the results are available, they will be submitted in a supplemental submission.The other three times referred to in the b5 will be sent in a separate submission.The submission numbers will be sent when available.
Event or Problem Description
It was reported that there was a failure with the clearsight module.There was a blood pressure reading discrepancy when using the cs module during use.Troubleshooting was done by checking the ge monitor, checking the ge cables, and checking the non-invasive blood pressure reading on the ge monitor and then assessing calibration.The disposable devices were exchanged, but the same reading discrepancy occurred.The clinician exchanged the pressure controller and the heart reference sensor devices, but the same issue still occurred.By process of elimination the clearsight module and acumen cuff were not ruled out as suspect.This event occurred three other times.The acumen cuff report will be submitted in a separate submission.There was no patient harm or injury.The patient demographics were requested but not provided.There was no inappropriate patient treatment administered.
Additional Manufacturer Narrative
The report id numbers are available to link these mdr submissions, 2015691-2024-05228, 2015691-2024-05229, 2015691-2024-05230, 2015691-2024-05231.The device history record review was completed and all manufacturing inspections passed with no non conformances.The product has been received and is being evaluated.When the evaluation results are available a supplemental report will be submitted.
Additional Manufacturer Narrative
The clearsight module was returned and evaluated.The evaluation found that when the clearsight module was connected to a known good working hemosphere monitoring system for testing three times, that each time there were no error messages noted.A normal blood pressure reading and waveform display were able to be obtained.A visual inspection found no physical damage to the device.There was no defect found.The reported issue could not be confirmed.The engineering evaluation was completed.The reported event could not be confirmed or replicated during the analysis, as the device responded appropriately during testing.Since the complaint was not confirmed there was not sufficient evidence to determine if this complaint was related to manufacturing, design, and/or labeling.It is not known if any procedural factors may have contributed to the event.Complaint histories for all reported events are reviewed against trending control limits on a monthly basis and any excursions above the control limits are assessed and documented as part of this monthly review.

• Brand Name: CLEARSIGHT MODULE
• Common Device Name: CLEARSIGHT MODULE
• Manufacturer (Section D): EDWARDS LIFESCIENCES; one edwards way; irvine CA 92614
• Manufacturer (Section G): EDWARDS LIFESCIENCES; one edwards way; irvine CA 92614
• Manufacturer Contact: katheryn cespedes ; 1 edwards way; irvine, CA 92614 ; 9492017706
• MDR Report Key: 19712789
• Report Number: 2015691-2024-05228
• Device Sequence Number: 8777817
• Product Code: DQK
• UDI-Device Identifier: 00690103202762
• UDI-Public: (01)00690103202762(11)230628
• Combination Product (Y/N): N
• Initial Reporter State: SC
• Initial Reporter Country: US
• PMA/510(K) Number: K201446
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Nurse
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 09/10/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: HEMCSM10
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/20/2024
• Supplement Date Received by Manufacturer: 07/10/2024; 09/03/2024
• Initial Report FDA Received Date: 07/10/2024
• Supplement Report FDA Received Date: 08/05/2024; 09/10/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/28/2023
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown