BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HURRYCANE

    MDR report key: 11831574 · Received May 14, 2021

    Report

    Report Number
    MW5101371
    Event Type
    Malfunction
    Date Received
    May 14, 2021
    Date of Event
    May 11, 2021
    Report Date
    May 12, 2021
    Manufacturer
    HURRYWORKS LLC
    Product Code
    KHY
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    WHILE WALKING WITH A HURRYCANE, THE HANDLE SEPARATED FROM THE SHAFT OF THE CANE. FORTUNATELY, I WAS ABLE TO BALANCE MYSELF AND NOT FALL. FDA SAFETY REPORT ID # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    725660 HURRYCANE CANE, SAFETY WALK KHY HURRYWORKS LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR