BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 29 STRETCHER 8/00

    MDR report key: 1830063 · Received September 7, 2010

    Report

    Report Number
    1831750-2010-02117
    Event Type
    Malfunction
    Date Received
    September 7, 2010
    Date of Event
    August 12, 2010
    Report Date
    August 12, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN A SERVICE REPORT THAT THE BRAKES WERE NOT FUNCTIONING TO SPECIFICATION. THERE WAS NO PATIENT INVOLVEMENT AND NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENAISSANCE 29 STRETCHER 8/00 HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1711 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA