BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIVONA MID-RANGE AIRE-CUF EXTRA LENGTH FIXED HYPERFLEX ADULT TRACHEOSTOMY TUBE

    MDR report key: 1951261 · Received December 13, 2010

    Report

    Report Number
    2183502-2010-00572
    Event Type
    Malfunction
    Date Received
    December 13, 2010
    Date of Event
    November 10, 2010
    Report Date
    December 7, 2010
    Manufacturer
    SMITHS MEDICAL ASD, INC.
    Product Code
    JOH
    PMA / PMN Number
    K081440
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    CUSTOMER HAS NOT YET RETURNED THE DEVICE TO THE MFR FOR DEVICE EVAL. WHEN AND IF THE DEVICE BECOMES AVAILABLE AND IS RETURNED AND EVALUATED, THE MFR WILL FILE A FOLLOW-UP REPORT DETAILING THE RESULTS OF THE EVAL.

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED THAT ALLEGES THAT THE TRACHEOSTOMY TUBE WAS DEFLATING AT THE CUFF AFTER AN UNK AMOUNT OF TIME IN SITU. REPLACEMENT WAS REQUIRED. NO INCIDENT RELATED MEDICAL SEQUELAE WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIVONA MID-RANGE AIRE-CUF EXTRA LENGTH FIXED HYPERFLEX ADULT TRACHEOSTOMY TUBE JOH-TRACHEOSTOMY TUBE JOH SMITHS MEDICAL ASD, INC. NA 1563933

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK