BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUICKIE 3RX WHEELCHAIR

    MDR report key: 91569 · Received May 15, 1997

    Report

    Report Number
    2082643-1997-00744
    Event Type
    Malfunction
    Date Received
    May 15, 1997
    Report Date
    May 14, 1997
    Manufacturer
    QUICKIE DESIGNS, INC.
    Product Code
    IOR
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ND, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DEALER CLAIMS THE X-TUBE IS BROKEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUICKIE 3RX WHEELCHAIR WHEELCHAIR, MECHANICAL IOR QUICKIE DESIGNS, INC. NA P/N-672616

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other