BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 1963967 · Received January 12, 2011

    Report

    Report Number
    1831750-2011-00334
    Event Type
    Malfunction
    Date Received
    January 12, 2011
    Date of Event
    December 13, 2010
    Report Date
    December 14, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV.
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT AN AMBULANCE CONTAINING A POWER-PRO XT WAS INVOLVED IN A CRASH WHICH RESULTED IN DAMAGE TO THE MOUNTING ASSEMBLY. THE CATCH DOES NOT FUNCTION UNLESS THE STRETCHER IS SLAMMED IN FORCIBLY AND EVEN THEN IT STILL MAY NOT CATCH AS A RESULT OF THIS ACCIDENT. THERE WAS NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES 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