BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 2823567 · Received October 8, 2012

    Report

    Report Number
    1831750-2012-10452
    Event Type
    Malfunction
    Date Received
    October 8, 2012
    Date of Event
    September 19, 2012
    Report Date
    September 19, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    HEIGHT ADJUSTMENT RACKS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEIGHT ADJUSTMENT RACKS WERE BENT. THE CUSTOMER REPORTED THAT THEY DID NOT KNOW IF THERE WAS NAY PT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1