MAUDE Adverse Event Report: Medtronic Ireland Micra¿ VR2; LEADLESS PACEMAKER

Model Number	MC2VR01-DELSYS
Medical Device Problem Code	Deformation Due to Compressive Stress (2889)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/17/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that during implant, the delivery system sheath kinking whole crossing valve from the internal jugular approach.A new micra was implanted with the femoral approach. no patient complications have been reported as a result of this event.
Additional Manufacturer Narrative
Product event summary: the full delivery system was returned and analyzed.The delivery system outer shaft was kinked/buckled.The delivery system tether was broken/cut/pulled apart.The delivery system inner shaft was mechanically kinked/bent.Visual analysis of the delivery system ind icated damage during use.The analyst noted the full delivery system was returned with the device, tether, and tether pin separated from the delivery system.The tether was cut.The outer shaft was kink/buckled at 6.5 cm from the distal end of the delivery system.The inner shaft was kinked at 3 cm from the distal end of the recapture cone.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: Micra¿ VR2
• Common Device Name: LEADLESS PACEMAKER
• Manufacturer (Section D): Medtronic Ireland; parkmore business park west; galway ; EI
• Manufacturer (Section G): Medtronic Ireland; parkmore business park west; galway ; EI
• Manufacturer Contact: gerard torenvliet ; 8200 coral sea st ne; mounds view, MN 55112--439 ; +1(763)526-9277
• MDR Report Key: 50881019
• Report Number: 9612164-2026-04801
• Device Sequence Number: 9826542
• Product Code: PNJ
• UDI-Device Identifier: 00763000078683
• UDI-Public: (01)00763000078683(17)270928
• Combination Product (Y/N): N
• Initial Reporter State: OR
• Initial Reporter Country: US
• PMA/510(K) Number: P150033
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 09/24/2026

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: MC2VR01-DELSYS
• Device Catalogue Number: MC2VR01-DELSYS
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 09/18/2026
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/22/2026
• Initial Report FDA Received Date: 09/24/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/13/2026
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Age: 65 YR
• Patient Sex: Male