BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HANDICARE STAIRLIFTS

    MDR report key: 8345344 · Received February 15, 2019

    Report

    Report Number
    3013423626-2019-00007
    Event Type
    Malfunction
    Date Received
    February 15, 2019
    Date of Event
    January 17, 2019
    Report Date
    February 15, 2019
    Manufacturer
    HANDICARE STAIRLIFTS B.V
    Product Code
    PCD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    UNIT SMOKED FROM PCB ON FIRST RUN DOWN COULD HAVE BEEN PINCHED WIRES FROM INSTALL. SHOULD BE INSPECTED WHEN RETURNED. NO INJURIES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    135556 HANDICARE STAIRLIFTS STAILIFTS PCD HANDICARE STAIRLIFTS B.V

    Patients

    Seq Age Sex Outcome Treatment
    1