BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 1894658 · Received November 5, 2010

    Report

    Report Number
    1831750-2010-03533
    Event Type
    Malfunction
    Date Received
    November 5, 2010
    Date of Event
    July 13, 2010
    Report Date
    July 13, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THROUGH SERVICE REPORT THAT A NEW TRIGGER LOCK AND CROSSBAR RELEASE HANDLE ARE NEEDED. NO ADVERSE HAVE BEEN REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1