BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GYNNIE OB-GYN STRETCHER

    MDR report key: 2963546 · Received February 15, 2013

    Report

    Report Number
    0001831750-2013-01188
    Event Type
    Malfunction
    Date Received
    February 15, 2013
    Date of Event
    January 23, 2013
    Report Date
    January 23, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    BRAKE CAM.

    Description of Event or Problem · 1

    IT WAS REPORTED BY REPAIR WORK ORDER THAT THE FOOT END BRAKES WERE NOT LOCKING DUE TO MALFUNCTIONED BRAKE CAMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    68107 GYNNIE OB-GYN STRETCHER STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1061

    Patients

    Seq Age Sex Outcome Treatment
    1