BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OB-GYN STRETCHER

    MDR report key: 1890463 · Received October 27, 2010

    Report

    Report Number
    1831750-2010-03307
    Event Type
    Malfunction
    Date Received
    October 27, 2010
    Date of Event
    August 23, 2010
    Report Date
    August 23, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKES ON THE HEAD END WERE NOT WORKING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OB-GYN STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL DIVISION 1060 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA