BEUDAMED
    FDA Adverse Event Injury Summary report: N

    C.R. BARD, INC

    MDR report key: 407644 · Received July 24, 2002

    Report

    Report Number
    407644
    Event Type
    Injury
    Date Received
    July 24, 2002
    Date of Event
    July 21, 2002
    Report Date
    July 24, 2002
    Manufacturer
    CR BARD INC
    Product Code
    KOD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CT, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    FOLEY CATHETER INSERTED. ATTEMPTED TO REMOVE FOLEY THREE DAYS LATER. BALLOON WOULD NOT DEFLATE-ATTEMPTED TO DEFLATE WITH SYRINGE AND BY CUTTING SIDE PORT. BALLOON REMAINED INTACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 C.R. BARD, INC FOLEY CATHETER I.C. KOD CR BARD INC 900016 76FMN008

    Patients

    Seq Age Sex Outcome Treatment
    1 94 YR Hospitalization