BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RENAISSANCE 29

    MDR report key: 1874996 · Received October 13, 2010

    Report

    Report Number
    1831750-2010-02824
    Event Type
    Malfunction
    Date Received
    October 13, 2010
    Date of Event
    September 10, 2010
    Report Date
    September 10, 2010
    Manufacturer
    STRYKER CORP. MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE FOOTEND OF THE STRETCHER WOULD NOT RAISE. THERE WAS NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENAISSANCE 29 HOSPITAL WHEELED STRETCHER FPO STRYKER CORP. MEDICAL DIVISION 1710 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA