BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIT SUR PIEDS ROUL SUP CHASSIS

    MDR report key: 2841666 · Received October 24, 2012

    Report

    Report Number
    1831750-2012-11163
    Event Type
    Malfunction
    Date Received
    October 24, 2012
    Date of Event
    September 19, 2012
    Report Date
    September 25, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE LATCH MECHANISM ON THE LEFT BED RAIL LET GO. IT WAS REPORTED THAT THERE WAS PT INVOLVEMENT, NO MEDICAL INTERVENTION, AND NO ADVERSE CONSEQUENCES. IT WAS REPORTED THAT THE EVENT DID NOT OCCUR DURING SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIT SUR PIEDS ROUL SUP CHASSIS A/C HOSPITAL BED FNL STRYKER MEDICAL FL14E3 NA

    Patients

    Seq Age Sex Outcome Treatment
    1