BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON-POWERED TRACTION APPARATUS AND ACCESSORIES

    MDR report key: 2884541 · Received December 22, 2012

    Report

    Report Number
    1525712-2012-03253
    Event Type
    Malfunction
    Date Received
    December 22, 2012
    Report Date
    December 21, 2012
    Manufacturer
    UNKNOWN
    Product Code
    HST
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    (B)(4). THE DEALER REPORTED THAT THE FULL BODY LIFT PREMIER SLING STRAP WAS FRAYING. THERE WAS NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NON-POWERED TRACTION APPARATUS AND ACCESSORIES 888.5850 HST UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other