BEUDAMED
    FDA Adverse Event Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 3033927 · Received April 3, 2013

    Report

    Report Number
    1531186-2013-01391
    Date Received
    April 3, 2013
    Report Date
    March 7, 2013
    Manufacturer
    NEW PROKIN
    Product Code
    INE
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE USER REPORTED THAT THE SLING USED ON THEIR PATIENT LIFT HAD WORN STRAPS THAT WERE TEARING. THIS ISSUE COULD CAUSE THE SLING TO BE UNSTABLE AND THE USER TO FALL OUT OF THE SLING DURING USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    137184 NON AC-POWERED PATIENT LIFT 880.5510 INE NEW PROKIN R101

    Patients

    Seq Age Sex Outcome Treatment
    1 52 Other