BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OEM STRETCHER CONFIGS

    MDR report key: 2191885 · Received July 29, 2011

    Report

    Report Number
    1831750-2011-07870
    Event Type
    Malfunction
    Date Received
    July 29, 2011
    Date of Event
    July 1, 2011
    Report Date
    July 1, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE WHEELS WERE COMING APART. THE CUSTOMER COULD NOT DETERMINE WHETHER THERE WAS PT INVOLVEMENT, HOWEVER NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OEM STRETCHER CONFIGS HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0722 NA

    Patients

    Seq Age Sex Outcome Treatment
    1