BEUDAMED
    FDA Adverse Event Summary report: N

    SKYTRON SURGICAL LIGHT

    MDR report key: 84382 · Received July 2, 1996

    Report

    Report Number
    84382
    Date Received
    July 2, 1996
    Manufacturer
    SKYTRON DIV, THE KMW GROUP
    Product Code
    FQP
    Report Source
    User Facility report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    DR REPOSITIONED OVERHEAD SPOT LIGHTS AND PAINT CHIPS FELL OFF THE LIGHTS ONTO THE STERILE FIELD PER THE DR. STERILE FIELD REDRAPED AT AT SITE WITH STERILE TOWELS. ALL SCRUBBED PERSONNEL CHANGED GLOVES AND WOUND IRRIGATED WELL WITH 1NACL WITH 50,000 UNITS BACITRACIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SKYTRON SURGICAL LIGHT SURGICAL LIGHT FQP SKYTRON DIV, THE KMW GROUP KR56 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *