FDA Adverse Event Injury Summary report: N

CAPSUREFIX NOVUS LEAD MRI SURESCAN

MDR report key: 25246474 · Received May 21, 2026

Report

Report Number
2649622-2026-15094
Event Type
Injury
Date Received
May 21, 2026
Date of Event
April 22, 2026
Report Date
May 21, 2026
Manufacturer
MEDTRONIC PUERTO RICO VILLALBA
Product Code
DTB
UDI-DI
00643169550766
PMA / PMN Number
P930039
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

CONTINUATION OF D10: 0155 LEAD IMPLANTED: (B)(6) 2001 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.

Description of Event or Problem · 0

IT WAS REPORTED THAT APPROXIMATELY ONE MONTH POST IMPLANT THE PATIENT EXPERIENCED A POCKET INFECTION WITH DISCOMFORT, PURULENT DISCHARGE/PUS, REDNESS, SWELLING, AND WOUND DEHISCENCE. THE LEADS WERE CUT, AND THE ICD WAS REMOVED. A LEADLESS IMPLANTABLE PULSE GENERATOR (IPG) WAS IMPLANTED. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
241142 CAPSUREFIX NOVUS LEAD MRI SURESCAN PERMANENT PACEMAKER ELECTRODE DTB MEDTRONIC PUERTO RICO VILLALBA 5076-52 00643169550766

Patients

Seq Age Sex Outcome Treatment
1 91 YR Male Hospitalization| R DDPA2D1 ICD