BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER LOAD

    MDR report key: 3143310 · Received June 3, 2013

    Report

    Report Number
    0001831750-2013-05025
    Event Type
    Malfunction
    Date Received
    June 3, 2013
    Date of Event
    May 7, 2013
    Report Date
    May 7, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE RELEASE ARMS WILL NOT RELEASE THE COT DUE TO THE MAGNET MOVER AND COMPRESSION SPRING FALLING OUT. THIS ONLY AFFECTED THE UNIT DURING POWERED OPERATION. THE UNIT WAS STILL FULLY OPERATIONAL IN MANUAL MODE IN WHICH A COT COULD STILL BE LOADED AND UNLOADED FROM THE AMBULANCE.

    Description of Event or Problem · 1

    IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE RELEASE ARMS WILL NOT RELEASE THE COT DUE TO THE MAGNET MOVER AND COMPRESSION SPRING FALLING OUT. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Description of Event or Problem · 1

    IT WAS REPORTED VIA REPAIR WORK ORDER THAT THE RELEASE ARMS WILL NOT RELEASE THE COT DUE TO THE MAGNET MOVER AND COMPRESSION SPRING FALLING OUT. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    244147 POWER LOAD STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1