BEUDAMED
    FDA Adverse Event Other Summary report: N

    CR BARD CATHETER

    MDR report key: 375292 · Received January 30, 2002

    Report

    Report Number
    375292
    Event Type
    Other
    Date Received
    January 30, 2002
    Date of Event
    December 28, 2001
    Report Date
    January 28, 2002
    Manufacturer
    C.R. BARD, INC
    Product Code
    KOD
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THE PT WAS ADMITTED FOR A TOTAL ABDOMINAL HYSTERECTOMY. A FOLEY CATHETER WAS INSERTED THE NEXT DAY, THE FOLEY WAS TO BE REMOVED. THE BALLOON WOULD NOT DEFLATE, A NEEDLE WAS PLACED TRANSURETRALLY, BALLOON WAS ASPIRATED. FOLEY WAS ASPIRATED. FOLEY WAS REMOVED. THE PT EXPERIENCED A SMALL AMOUNT OF URETERAL BLEEDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CR BARD CATHETER FOLEY CATHETER KOD C.R. BARD, INC 16F UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Other