BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BUTTON REPLACEMENT GASTROSTOMY DEVICE

    MDR report key: 17902 · Received September 9, 1994

    Report

    Report Number
    17902
    Event Type
    Malfunction
    Date Received
    September 9, 1994
    Date of Event
    August 31, 1994
    Report Date
    September 9, 1994
    Manufacturer
    INTERVENTIONAL PRODUCT DIV. C.R. BARD, INC.
    Product Code
    KNT
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DEFECTIVE VALVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BUTTON REPLACEMENT GASTROSTOMY DEVICE BUTTON REPLACEMENT GASTROSTOMY DEVICE KNT INTERVENTIONAL PRODUCT DIV. C.R. BARD, INC. 43EEA003

    Patients

    Seq Age Sex Outcome Treatment
    1 *