BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HANDICARE

    MDR report key: 18166128 · Received November 17, 2023

    Report

    Report Number
    3013423626-2023-00002
    Event Type
    Injury
    Date Received
    November 17, 2023
    Date of Event
    September 27, 2023
    Report Date
    November 17, 2023
    Manufacturer
    HANDICARE STAIRLIFTS B.V.
    Product Code
    PCD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    WE RECEIVED COMMUNICATION FROM FDA THAT AN MDR WAS SUBMITTED ON OUR BEHALF BY THE END USER WITH THE FOLLOWING DESCRIPTION: "STAIRLIFT STOPPED PART WAY UP AND REQUIRED FIRST RESPONDERS TO RESCUE ME."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    674278 HANDICARE POWERED STAIRWAY CHAIR LIFT PCD HANDICARE STAIRLIFTS B.V.

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown