BEUDAMED
    FDA Adverse Event Summary report: N

    VISCOAT

    MDR report key: 18802 · Received January 6, 1995

    Report

    Report Number
    MW1004651
    Date Received
    January 6, 1995
    Date of Event
    December 27, 1994
    Manufacturer
    ALCON SURGICAL, INC.
    Product Code
    LZP
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IN THE SURGERY UNIT AT THE TIME THE DR WAS TO USE THIS DEVICE, IT WAS NOTED THAT THE PLUNGER ON THE SYRINGE WAS DEFECTIVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VISCOAT LZP ALCON SURGICAL, INC. V4570

    Patients

    Seq Age Sex Outcome Treatment
    1 *