BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA 850 BED

    MDR report key: 1162849 · Received September 9, 2008

    Report

    Report Number
    1824206-2008-03357
    Event Type
    Malfunction
    Date Received
    September 9, 2008
    Date of Event
    August 15, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE LOSS OF TRENDELENBURG/REVERSE TRENDELENBURG HAS THE POTENTIAL TO CAUSE SERIOUS INJURY OR DEATH. THE TECHNICIAN REPLACED THE PILOT LINK IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    AN ACCOUNT STATED THAT A BED WAS FOUND IN STORAGE THAT WOULD NOT GO INTO TRENDELENBURG POSITION. THERE WAS NO PATIENT INVOLVEMENT IN THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA 850 BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P850 N/A

    Patients

    Seq Age Sex Outcome Treatment
    1