BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRETCHER CHAIR

    MDR report key: 2091198 · Received April 20, 2011

    Report

    Report Number
    1831750-2011-03839
    Event Type
    Malfunction
    Date Received
    April 20, 2011
    Date of Event
    March 25, 2011
    Report Date
    March 25, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: LATCH HOUSING INSERT.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE LOCKING KNOB WAS BROKEN ON THE LEFT SIDE RAIL. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRETCHER CHAIR STRETCHER, WHEELED FPO STRYKER MEDICAL 5050 NA

    Patients

    Seq Age Sex Outcome Treatment
    1