BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 2915150 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12650
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 14, 2012
    Report Date
    November 14, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LIFT MOTOR LIMIT WAS NOT SET. THIS ISSUE WAS RESOLVED FOR THE CUSTOMER BY RESETTING HEIGHT LIMITS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS REDUCED RANGE OF MOTION AT THE FOOT END LIFT AND THERE WAS NO POWER AT THE AUXILIARY OUTLET. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1