BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FULL CUFF FOREARM CRUTCH

    MDR report key: 18372407 · Received December 20, 2023

    Report

    Report Number
    MW5149427
    Event Type
    Injury
    Date Received
    December 20, 2023
    Date of Event
    December 14, 2023
    Report Date
    December 20, 2023
    Manufacturer
    KX MEDICAL LLC.
    Product Code
    IPR
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    003
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    CALLER STATED HE PURCHASED A CRUTCH TWO AND HALF YEARS AGO AND IT BROKE. HE CONTACTED THE MANUFACTURER AND IT WAS REPLACED, UNFORTUNATELY THE REPLACEMENT BROKE THE EXACT SAME WAY AND EACH TIME HE FELL. HE SAYS HE USE THIS CRUTCH FOR AMBULATORY PURPOSE. CALLER BELIEVES THE CRUTCHES ARE DEFECTIVE. REF REPORT: MW5149426.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1750846 FULL CUFF FOREARM CRUTCH CRUTCH IPR KX MEDICAL LLC. SKD

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Male Required Intervention