BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STETHOSCOPE

    MDR report key: 9139977 · Received October 1, 2019

    Report

    Report Number
    9139977
    Event Type
    Malfunction
    Date Received
    October 1, 2019
    Date of Event
    August 27, 2019
    Report Date
    August 29, 2019
    Manufacturer
    BARRINGTON VENTURES, LTD
    Product Code
    LDE
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MT
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THE NURSE WENT TO GO USE THE PURPLE ISOLATION STETHOSCOPE ON THE PATIENT AND SHE NOTICED THAT THE BLADDER WAS CRACKED ON THE EDGE. THE PATIENT WAS NOT HURT IN THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    932270 STETHOSCOPE STETHOSCOPE, MANUAL LDE BARRINGTON VENTURES, LTD

    Patients

    Seq Age Sex Outcome Treatment
    1 300 DA