BEUDAMED
    FDA Adverse Event Other Summary report: N

    QUICKIE P200 WHEELCHAIR

    MDR report key: 267704 · Received March 7, 2000

    Report

    Report Number
    2082643-2000-00228
    Event Type
    Other
    Date Received
    March 7, 2000
    Date of Event
    February 10, 2000
    Report Date
    February 23, 2000
    Manufacturer
    SUNRISE MEDICAL MPD
    Product Code
    ITI
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    SERVICE PERSONNEL

    Narratives

    Description of Event or Problem · 1

    REPORTER CLAIMS THE END USER CAUGHT THE FINGER WITH THE RING INSIDE THE CONTROLLER CABLE WHICH CAUSED IT TO SHORT. REPORTER FEELS THIS IS BECAUSE END USER JAMMED A SCREWDRIVER INTO THE CABLE TO STRAIGHTEN THE PRONGS. END USER CLAIMS REPORTER BURNED THE FINGER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUICKIE P200 WHEELCHAIR WHEELCHAIR, POWERED ITI SUNRISE MEDICAL MPD NA P/N 139134

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other