BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1853048 · Received September 21, 2010

    Report

    Report Number
    1831750-2010-02464
    Event Type
    Malfunction
    Date Received
    September 21, 2010
    Date of Event
    September 2, 2010
    Report Date
    September 2, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FNL
    Removal / Correction Number
    Z-1685-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DE, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    FACILITY REPORTED AND ORDERED PARTS FOR REPAIR AND RETURN TO SERVICE.

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT, THE BRAKES ARE NOT HOLDING ON THE UNIT. NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1