BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 2000247 · Received February 18, 2011

    Report

    Report Number
    1831750-2011-01596
    Event Type
    Malfunction
    Date Received
    February 18, 2011
    Date of Event
    January 21, 2011
    Report Date
    January 21, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: MOTION INTERRUPT PAN.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE BED WOULD NOT LOWER PROPERLY DUE TO THE MOTION INTERRUPT PAN. ADDITIONALLY, IT WAS REPORTED THAT WHILE CHECKING TO MAKE SURE THE POWER CORD WAS PLUGGED IN, A NURSE AIDE INADVERTENTLY ENGAGED THE MANUAL CPR RELEASE. WHILE TRYING TO CATCH THE PATIENT, SHE RECEIVED A CUT ON HER FINGER. THE BED WAS INSPECTED FOR SHARP EDGES, BUT NONE WERE FOUND. NO MEDICAL INTERVENTION WAS REQUIRED. THERE WAS PATIENT INVOLVEMENT, BUT THE PATIENT EXPERIENCED NO ADVERSE CONSEQUENCES FROM THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE II MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1