BEUDAMED
    FDA Adverse Event Other Summary report: N

    LMA CLASSIC

    MDR report key: 391636 · Received April 29, 2002

    Report

    Report Number
    391636
    Event Type
    Other
    Date Received
    April 29, 2002
    Date of Event
    March 15, 2002
    Report Date
    March 28, 2002
    Manufacturer
    LMA NORTH AMERICA, INC.
    Product Code
    CAE
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THIS PT HAD SURGERY IN 2002. A LARYNGEAL MASK AIRWAY WAS USED DURING THE SURGERY. POST-OPERATIVELY, THE PT EXPRESSED A SEVERE SORE THROAT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LMA CLASSIC LARYNGEAL MASK AIRWAY CAE LMA NORTH AMERICA, INC. LMA SIZE 4 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 39 YR Other