FDA Adverse Event Injury Summary report: N

SELECTSECURE MRI SURESCAN

MDR report key: 24995411 · Received April 27, 2026

Report

Report Number
2649622-2026-11856
Event Type
Injury
Date Received
April 27, 2026
Date of Event
April 8, 2026
Report Date
April 27, 2026
Manufacturer
MEDTRONIC PUERTO RICO VILLALBA
Product Code
NVN
UDI-DI
00763000740269
PMA / PMN Number
P030036
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

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 ON THE SAME DAY AS IMPLANT THE RIGHT VENTRICULAR (RV) LEFT BUNDLE BRANCH LEAD EXHIBITED HIGH THRESHOLD POST ATR IOVENTRICULAR JUNCTION (AVJ) ABLATION. THE PATIENT EXPERIENCED SYMPTOMS AND THE SURGEON SUSPECTS LOCAL BURNED TISSUE CAUSE HIGH THRESHOLD OBSERVED POST ABLATION. THE LEAD WAS EXPLANTED AND REPLACED. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
26176 SELECTSECURE MRI SURESCAN DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) NVN MEDTRONIC PUERTO RICO VILLALBA 383069 00763000740269

Patients

Seq Age Sex Outcome Treatment
1 85 YR Female Hospitalization| R W1DR01 IPG, 383059 LEAD.