BEUDAMED
    FDA Adverse Event Summary report: N

    SUCTION CATHETER, 14 FR

    MDR report key: 10756 · Received January 4, 1994

    Report

    Report Number
    MW1000281
    Date Received
    January 4, 1994
    Date of Event
    December 9, 1993
    Manufacturer
    SUPERIOR HEALTHCARE GROUP, INC.
    Product Code
    BSY
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    A MAN WAS BEING TRACHEALLY SUCTIONED BY HIS WIFE. BLEEDING OCCURRED AS A RESULT OF THE SUCTIONING PROCEDURE. WHEN THE CATHETER WAS WITHDRAWN FROM THE TRACH TUBE, IT WAS INSPECTED AND A "JAGGED EDGE" WAS SEEN. THE CATHETER WAS DISCARDED, NO REPORT WAS MADE BY THE FAMILY UNTIL 12/23/93 WHEN A ROUTINE ORDER FOR SUPPLIES WAS PLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUCTION CATHETER, 14 FR BSY SUPERIOR HEALTHCARE GROUP, INC. 31400 3292B

    Patients

    Seq Age Sex Outcome Treatment
    1 *