BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 1875019 · Received October 13, 2010

    Report

    Report Number
    1831750-2010-02810
    Event Type
    Malfunction
    Date Received
    October 13, 2010
    Date of Event
    September 17, 2010
    Report Date
    September 17, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    OTHER: WELDMENT.

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THERE IS A BROKEN OUTER TUBE WELDMENT. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWER PRO AMBULANCE COT STRETCHER WHEELED INK STRYKER CORP., MEDICAL DIV 6500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1