MAUDE Adverse Event Report: MPRI CAPSUREFIX NOVUS LEAD MRI SURESCAN; PERMANENT PACEMAKER ELECTRODE

Model Number 5076-45

Device Problem Under-Sensing (1661)

Patient Problem Insufficient Information (4580)

Event Date 02/23/2024

Event Type  Death  

Event Description

It was reported that the patient passed away.It was noted that the right atrial (ra) lead exhibited intermittent undersensing, triggering the false termination of events.It was further observed the cardiac resynchronization therapy defibrillator (crt-d) appropriately treated a ventricular tachycardia (vt) episode, but the arrhythmia continued beneath the detection rate.

Manufacturer Narrative

Continuation of d10: dtma1d1 implanted: (b)(6) 2017; medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.

• Brand Name: CAPSUREFIX NOVUS LEAD MRI SURESCAN
• Type of Device: PERMANENT PACEMAKER ELECTRODE
• Manufacturer (Section D): MPRI; road 149 km 56.3; villalba PR 00766
• Manufacturer (Section G): MPRI; road 149 km 56.3; villalba PR 00766
• Manufacturer Contact: paula bixby ; 8200 coral sea st ne; mounds view, MN 55112 ; 7635055378
• MDR Report Key: 19006726
• MDR Text Key: 338942440
• Report Number: 2649622-2024-08672
• Device Sequence Number: 1
• Product Code: DTB
• UDI-Device Identifier: 00681490124799
• UDI-Public: 00681490124799
• Combination Product (y/n): Y
• Reporter Country Code: US
• PMA/PMN Number: P930039
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 03/29/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/29/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Device Expiration Date: 11/15/2009
• Device Model Number: 5076-45
• Device Catalogue Number: 5076-45
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 03/02/2024
• Date Device Manufactured: 11/23/2007
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: 419388 LEAD, 694758 LEAD,
• Patient Outcome(s): Death
• Patient Age: 71 YR
• Patient Sex: Female