BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ATOMIC OR TABLE

    MDR report key: 908324 · Received August 30, 2007

    Report

    Report Number
    MW5003627
    Event Type
    Injury
    Date Received
    August 30, 2007
    Date of Event
    August 23, 2007
    Report Date
    August 30, 2007
    Manufacturer
    *
    Product Code
    EYH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    AT THE END OF THE UROLOGY CASE, JUST PRIOR TO MOVING THE PT ONTO A STRETCHER, THE CYSTO BED STARTED TO LOWER AT THE FOOT END TOWARD THE FLOOR. STAFF WAS ABLE TO MOVE PT WITHOUT INCIDENT TO THE STRETCHER. THE CYSTO BED WAS NOT ABLE TO OPERATE NORMALLY, SO IT WAS REMOVED FROM OR AND TAGGED FOR REPAIR. DIAGNOSIS: CYSTO CASES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ATOMIC OR TABLE CYSTO BED EYH * 056450 *

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Disability