BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 2760296 · Received September 20, 2012

    Report

    Report Number
    1831750-2012-09977
    Event Type
    Malfunction
    Date Received
    September 20, 2012
    Date of Event
    August 23, 2012
    Report Date
    August 23, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: MOTION INTERRUPT PAN.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE AC POWER CORD WAS TORN NEAR THE PLUG END WITH EXPOSED WIRES, AND THE MOTION INTERRUPT PAN WAS MISSING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    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