BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 2253936 · Received August 11, 2011

    Report

    Report Number
    1831750-2011-08568
    Event Type
    Malfunction
    Date Received
    August 11, 2011
    Date of Event
    July 14, 2011
    Report Date
    July 14, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    HEIGHT ADJUSTMENT RACKS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT BOTH OF THE HEIGHT ADJUSTMENT RACKS WERE BENT. THE CUSTOMER COULD NOT DETERMINE WHETHER THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO R-3 AMBULANCE COT STRETCHER, WHEELED INK STRYKER MEDICAL 6082 NA

    Patients

    Seq Age Sex Outcome Treatment
    1