BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SM204 M-SERIES W/BIG WHEEL

    MDR report key: 2190551 · Received February 27, 2007

    Report

    Report Number
    1831750-2007-00009
    Event Type
    Malfunction
    Date Received
    February 27, 2007
    Date of Event
    January 28, 2007
    Report Date
    January 28, 2007
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    WHILE REPAIRING A STRETCHER FOR A DRIFTING JACK, IT WAS NOTICED THAT CHROME WAS PEELING ON THE SIDERAIL OF THE STRETCHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM204 M-SERIES W/BIG WHEEL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIVISION 1015 NA

    Patients

    Seq Age Sex Outcome Treatment
    1