BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VISCOAT

    MDR report key: 37232 · Received September 11, 1996

    Report

    Report Number
    MW1009898
    Event Type
    Malfunction
    Date Received
    September 11, 1996
    Date of Event
    September 9, 1996
    Report Date
    September 9, 1996
    Manufacturer
    ALCON SURGICAL, INC.
    Product Code
    LZP
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    CANNULA HAD HAIRS ON CONTAINER WHEN OPENED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VISCOAT VISCOELASTIC SURGICAL AID LZP ALCON SURGICAL, INC. * 512858

    Patients

    Seq Age Sex Outcome Treatment
    1 *