BEUDAMED
    FDA Adverse Event Death Summary report: N

    SPRINT QUATTRO SECURE MRI SURESCAN

    MDR report key: 22906385 · Received August 27, 2025

    Report

    Report Number
    2649622-2025-23466
    Event Type
    Death
    Date Received
    August 27, 2025
    Date of Event
    July 5, 2023
    Report Date
    August 27, 2025
    Manufacturer
    MEDTRONIC PUERTO RICO VILLALBA
    Product Code
    LWS
    UDI-DI
    00613994249890
    PMA / PMN Number
    P920015
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    003

    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 THE PATIENT IS DECEASED. THE PATIENT'S SPOUSE INDICATED THAT DURING USE OF THE CARDIAC RESYNCHRONIZATION THERAPY DEFIBRILLATOR (CRT-D) SYSTEM THE PATIENT¿S LEGS BEGAN TO SEEP FLUID AND FORM BLISTERS AND WAS INSTRUCTED BY A PHYSICIAN TO ADMINISTER DIURETIC TWO TIMES A DAY. ADDITIONALLY, IT WAS STATED THAT LATER THE PATIENT EXPERIENCED A FALL AND COULD NO LONGER STAND. THE PATIENT PRESENTED TO THE HOSPITAL, PROCEDURES AND TEST WERE PERFORMED AND THE PATIENT WAS DIAGNOSED WITH AN INFECTED DEVICE, AND THE INFECTION OF SEPSIS AND STAPH HAD SPREAD THROUGHOUT THE PATIENT¿S SYSTEM. IT WAS ALSO REPORTED THAT MANY PROCEDURES INCLUDING DIALYSIS WERE PERFORMED, HOWEVER, THE PATIENT SUBSEQUENTLY EXPIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1498441 SPRINT QUATTRO SECURE MRI SURESCAN IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT) LWS MEDTRONIC PUERTO RICO VILLALBA 694765 00613994249890

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Male Hospitalization| D| R 439888 LEAD, DTPA2Q1 CRT-D