BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUICKIE 2 WHEELCHAIR

    MDR report key: 180838 · Received August 6, 1998

    Report

    Report Number
    2082643-1998-01030
    Event Type
    Malfunction
    Date Received
    August 6, 1998
    Date of Event
    July 9, 1998
    Report Date
    August 6, 1998
    Manufacturer
    SUNRISE MEDICAL MPD
    Product Code
    IOR
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    SERVICE PERSONNEL

    Narratives

    Description of Event or Problem · 1

    REPORTER CLAIMS X-TUBE BROKE AT THE CENTER BOLT WHILE CHAIR WAS IN USE. NO INJURIES INVOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUICKIE 2 WHEELCHAIR WHEELCHAIR, MECHANICAL IOR SUNRISE MEDICAL MPD NA P/N-672816

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Other