BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 2963536 · Received February 15, 2013

    Report

    Report Number
    0001831750-2013-01196
    Event Type
    Malfunction
    Date Received
    February 15, 2013
    Date of Event
    January 23, 2013
    Report Date
    January 23, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY REPAIR WORK ORDER THAT THE CUSTOMER ALLEGED THAT THE HYDRUALICS WERE DRIFTING. UPON INSPECTION OF THE UNIT BY THE SERVICE TECHNICIAN, THE ALLEGED EVENT COULD NOT BE DUPLICATED ABND THE JACKS WERE FOUND TO BE WORKING TO SPECIFICATIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    66678 EYE SURGERY STRETCHER STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1089

    Patients

    Seq Age Sex Outcome Treatment
    1