BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 2974574 · Received February 22, 2013

    Report

    Report Number
    0001831750-2013-01455
    Event Type
    Malfunction
    Date Received
    February 22, 2013
    Date of Event
    January 28, 2013
    Report Date
    January 28, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    FOLLOW-UP SUBMITTED AS FURTHER INVESTIGATION DETERMINED THERE WAS ALSO A SIDERAIL STUCK IN THE LOW POSITION DUE TO A BENT TIMING LINK AND THE NURSE CALL WAS NOT WORKING DUE TO A DAMAGED CABLE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE GROUND PRONG WAS MISSING ON THE POWER CORD.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE GROUND PRONG WAS MISSING ON THE POWER CORD, A SIDERAIL WAS STUCK IN THE LOW POSITION DUE TO A BENT TIMING LINK, AND THE NURSE CALL WAS NOT WORKING DUE TO A DAMAGED CABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    77702 SECURE II MED/SURG BED BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1