BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIG WHEEL STRETCHER

    MDR report key: 2558664 · Received April 18, 2012

    Report

    Report Number
    1831750-2012-04170
    Event Type
    Malfunction
    Date Received
    April 18, 2012
    Date of Event
    March 20, 2012
    Report Date
    March 20, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    FOWLER.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER WAS NOT WORKING. NO SERIAL OR MODEL NUMBER WAS RECORDED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIG WHEEL STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1015 NA

    Patients

    Seq Age Sex Outcome Treatment
    1