BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    C.R. BARD, INC.

    MDR report key: 25397 · Received January 10, 1995

    Report

    Report Number
    25397
    Event Type
    Malfunction
    Date Received
    January 10, 1995
    Date of Event
    May 28, 1994
    Report Date
    August 10, 1994
    Manufacturer
    BARD UROLOGICAL DIVISION
    Product Code
    EYJ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    DC, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    ON ATTEMPT TO DEFLATE FOLEY CATHETER BALLOON, ONLY 5CC. OF FLUID COULD BE REMOVED. REMAINDER OF FLUID COULD NOT BE REMOVED FROM BALLOON BEFORE CATHETER WAS REMOVED FROM PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 C.R. BARD, INC. FOLEY CATHETER 16F EYJ BARD UROLOGICAL DIVISION

    Patients

    Seq Age Sex Outcome Treatment
    1 67 *