BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SUCTION CATHETER, 8F

    MDR report key: 10691 · Received December 29, 1993

    Report

    Report Number
    MW1000239
    Event Type
    Malfunction
    Date Received
    December 29, 1993
    Date of Event
    December 3, 1993
    Report Date
    December 16, 1993
    Manufacturer
    SUPERIOR HEALTHCARE GROUP, INC.
    Product Code
    BSY
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PRIOR TO SUCTIONING PT THE 8F SUCTION CATHETER BROKE NEAR THE THUMB PORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUCTION CATHETER, 8F BSY SUPERIOR HEALTHCARE GROUP, INC. 3161A

    Patients

    Seq Age Sex Outcome Treatment
    1 *