BEUDAMED
    FDA Adverse Event Other Summary report: N

    MAXI MOVE

    MDR report key: 3773603 · Received February 26, 2014

    Report

    Report Number
    1419652-2014-00053
    Event Type
    Other
    Date Received
    February 26, 2014
    Report Date
    January 28, 2014
    Manufacturer
    ARJOHUNTLEIGH MAGOG INC.
    Product Code
    FSA
    Report Source
    Distributor report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT AN INCIDENT OCCURRED AT A FACILITY WHERE THE CLIPS ON THE BOTTOM OF THE SLING BROKE. THIS WAS A 4-POINT REUSABLE SLING USED WITH A FLOOR LIFT MAXI MOVE. IT WAS MENTIONED THAT THE LEFT BOTTOM CLIP BROKE COMPLETELY AND THE RIGHT BOTTOM CLIP WAS DETERIORATING AND ON ITS WAY TO SNAPPING. THERE WAS NO INFO ABOUT POSSIBLE INJURIES SUSTAINED. REFERENCE MFR REPORT NUMBER: 9681684-2014-00015.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    119693 MAXI MOVE FSA ARJOHUNTLEIGH MAGOG INC.

    Patients

    Seq Age Sex Outcome Treatment
    1