BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 2981867 · Received February 27, 2013

    Report

    Report Number
    1525712-2013-01494
    Event Type
    Malfunction
    Date Received
    February 27, 2013
    Report Date
    February 1, 2013
    Manufacturer
    UNKNOWN
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    (B)(4). IT WAS REPORTED BY THE FACILITY STAFF THAT THE 9805P HYDRAULIC LIFT WOULD RAISE THE PATIENT. HOWEVER, IT WOULD SLOWLY DRIFT DOWN, NOT GIVING ENOUGH TIME TO TRANSPORT HER. THERE WAS NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    83749 NON AC-POWERED PATIENT LIFT 880.5510 FSA UNKNOWN 9805P

    Patients

    Seq Age Sex Outcome Treatment
    1 88 Other