BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWERED MOV CHAIR

    MDR report key: 1906209 · Received November 17, 2010

    Report

    Report Number
    1831750-2010-03916
    Event Type
    Malfunction
    Date Received
    November 17, 2010
    Date of Event
    March 12, 2010
    Report Date
    March 12, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    ITI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BATTERY IS BAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWERED MOV CHAIR POWERED PATIENT TRANSPORT ITI STRYKER CORP, MEDICAL DIVISION 12-000-00 NA

    Patients

    Seq Age Sex Outcome Treatment
    1