BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWERED WHEELCHAIR

    MDR report key: 2851937 · Received November 29, 2012

    Report

    Report Number
    1525712-2012-02491
    Event Type
    Malfunction
    Date Received
    November 29, 2012
    Report Date
    November 29, 2012
    Manufacturer
    INVACARE TAYLOR STREET
    Product Code
    ITI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4)- HAS BEEN INITIATED FOR THIS ISSUE. MODEL XXX, SERIAL NUMBER/DATE (B)(4) IS APPROXIMATELY XXXX OLD. THE OWNER'S MANUAL PART NUMBER 1023891, WAS ISSUED WITH THIS DEVICE. THE OWNER'S MANUAL IS ALSO FOUND ON-LINE AT INVACARE.COM. IT IS UNKNOWN IF THE CONSUMER HAS FULLY READ AND UNDERSTANDS THE OWNER'S MANUAL. DOCUMENTATION PROVIDES WARNINGS, CAUTIONS, AND INSTRUCTIONS FOR SAFELY USING THE DEVICE. IF THE CONSUMER DOES NOT UNDERSTAND THE WRITTEN WARNINGS, CAUTIONS OR INSTRUCTIONS THEN THEY SHOULD CONTACT INVACARE. THE CONSUMERS MEDICAL CONDITION, STABILITY AND MEDICATION REGIMEN ARE UNKNOWN. THE CONSUMER'S TECHNIQUE WHILE USING THE DEVICE IS UNKNOWN. THE MAINTENANCE HISTORY OF THE DEVICE IS UNKNOWN. THE MALFUNCTION HAS NOT BEEN CONFIRMED.

    Description of Event or Problem · 1

    DEALER STATED THAT THE WIRES ARE SEPARATING WHERE THE CHARGER CONNECTS TO THE JOYSTICK. A NEW JOYSTICK HAS BEEN SENT TO REPLACE AFFECTED PART UNDER WARRANTY. NO INJURY OR ILL EFFECT TO THE INVOLVED END USER. PLEASE NOTE ANY FURTHER INFORMATION OR SAMPLE ANALYSIS WILL BE FILED IN A SUPPLEMENTAL REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWERED WHEELCHAIR 890.3860 ITI INVACARE TAYLOR STREET TDXSR

    Patients

    Seq Age Sex Outcome Treatment
    1 32 Other