BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BARD FOLEY CATHETER

    MDR report key: 6053817 · Received October 21, 2016

    Report

    Report Number
    MW5065591
    Event Type
    Injury
    Date Received
    October 21, 2016
    Date of Event
    October 20, 2016
    Report Date
    October 21, 2016
    Manufacturer
    BARD MEDICAL DIVISION
    Product Code
    EZL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    FOLEY CATHETER LEAKING URINE. BALLOON CHECKED AND ONLY 5CC OF SALINE WAS FOUND. CATHETER REMOVED AND A NEW ONE REINSERTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    700554 BARD FOLEY CATHETER FOLEY CATHETER EZL BARD MEDICAL DIVISION

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Required Intervention