BEUDAMED
    FDA Adverse Event Summary report: N

    NON-POWERED TRACTION APPARATUS AND ACCESSORIES

    MDR report key: 2884412 · Received December 22, 2012

    Report

    Report Number
    1531186-2012-01843
    Date Received
    December 22, 2012
    Report Date
    December 20, 2012
    Manufacturer
    HL CORP. (SHENZHEN)
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DC, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    (B)(4). IT WAS REPORTED BY THE CONSUMER THAT THE 6630 BED RAILS WERE LOOSE, AND WHEN LOWERED IT JUST FLOPPED UPSIDE DOWN. 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 FNL HL CORP. (SHENZHEN) 6630

    Patients

    Seq Age Sex Outcome Treatment
    1 Other