BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTAGE SERIES 26

    MDR report key: 2861945 · Received October 31, 2012

    Report

    Report Number
    1831750-2012-11399
    Event Type
    Malfunction
    Date Received
    October 31, 2012
    Date of Event
    October 6, 2012
    Report Date
    October 5, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LEFT HAND SIDE RAIL WOULD NOT LATCH IN THE RAISED POSITION DUE TO A BROKEN WELD. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANTAGE SERIES 26 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1001 NA

    Patients

    Seq Age Sex Outcome Treatment
    1