BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MOV EVACUATION CHAIR

    MDR report key: 1928512 · Received November 24, 2010

    Report

    Report Number
    1831750-2010-04201
    Event Type
    Malfunction
    Date Received
    November 24, 2010
    Date of Event
    September 22, 2010
    Report Date
    September 22, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV
    Product Code
    FPP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UT, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE EVACUATION CHAIR HAD A BAD BATTERY. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MOV EVACUATION CHAIR EVACUATION CHAIR FPP STRYKER CORP, MEDICAL DIV NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1