BEUDAMED
    FDA Adverse Event Other Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1890815 · Received October 27, 2010

    Report

    Report Number
    1831750-2010-03292
    Event Type
    Other
    Date Received
    October 27, 2010
    Date of Event
    September 29, 2010
    Report Date
    September 29, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: FOWLER MOTOR IS LEAKING, HEADEND OF THE BED IS CROOKED AND DAMAGED. LITTER FRAME IS VERY BENT.

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE BED WAS DAMAGED BEYOND REPAIR. 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 DIV. 3002 EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1