BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE ACUTE CARE BED 3/01

    MDR report key: 1920601 · Received December 6, 2010

    Report

    Report Number
    1831750-2010-04541
    Event Type
    Malfunction
    Date Received
    December 6, 2010
    Date of Event
    October 11, 2010
    Report Date
    October 11, 2010
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL PANEL HAD A CRACK AND WAS UNABLE TO SCREW IN ON THE BOTTOM. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE ACUTE CARE BED 3/01 A/C POWERED HOSPITAL BED FNL 3000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1