BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 26 OBS 10/25/04

    MDR report key: 3021572 · Received March 26, 2013

    Report

    Report Number
    0001831750-2013-02506
    Event Type
    Malfunction
    Date Received
    March 26, 2013
    Date of Event
    February 12, 2013
    Report Date
    March 6, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE SIDE RAILS WERE DIFFICULT TO LATCH DUE TO A MISSING LATCH SPRING. THE SCREWS ON THE GAS CYLINDERS NEEDED ADJUSTMENT DUE TO BEING LOOSE. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    124314 RENAISSANCE 26 OBS 10/25/04 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1