BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 2774046 · Received September 26, 2012

    Report

    Report Number
    1831750-2012-10135
    Event Type
    Malfunction
    Date Received
    September 26, 2012
    Date of Event
    August 30, 2012
    Report Date
    August 30, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    SCREW JACK ASSEMBLY ON THE HED END LIFT HAD TO BE REPLACED.

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE HEAD LIFT WAS NOT MOVING AND WAS STUCK IN HIGH POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1