BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES

    MDR report key: 2143590 · Received June 2, 2011

    Report

    Report Number
    1831750-2011-05412
    Event Type
    Malfunction
    Date Received
    June 2, 2011
    Date of Event
    May 5, 2011
    Report Date
    May 5, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL LATCHING MECHANISM WAS NOT CATCHING EVERY TIME. IT IS UNK IF THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSPORT SERIES HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0721 NA

    Patients

    Seq Age Sex Outcome Treatment
    1