BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNIVERSAL MICROTOME

    MDR report key: 47987 · Received September 20, 1996

    Report

    Report Number
    2028159-1996-00172
    Event Type
    Malfunction
    Date Received
    September 20, 1996
    Report Date
    August 21, 1996
    Manufacturer
    ALCON LABORATORIES
    Product Code
    HQE
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    REPORTER ENCOUNTERED REQUENT POWER FAILURE MESSAGES. THERE WAS NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNIVERSAL MICROTOME VITREORETINAL SURGERY SYSTEM HQE ALCON LABORATORIES UMVS UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN