BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BARD LUBRICIOUS COATED RIBBED FOLEY CATHETER RIBBED PEDIATRI

    MDR report key: 199857 · Received November 30, 1998

    Report

    Report Number
    MW1015084
    Event Type
    Malfunction
    Date Received
    November 30, 1998
    Date of Event
    November 27, 1998
    Report Date
    November 30, 1998
    Manufacturer
    C R BARD, INC.
    Product Code
    KOD
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    BALLOON WOULD NOT DEFLATE WHEN READY TO REMOVE FROM PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD LUBRICIOUS COATED RIBBED FOLEY CATHETER RIBBED PEDIATRI 8 FR. 3CC RIBBED BALLOON FOLEY CATHETER KOD C R BARD, INC. * KD847

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other