BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 2081791 · Received April 13, 2011

    Report

    Report Number
    1831750-2011-03508
    Event Type
    Malfunction
    Date Received
    April 13, 2011
    Date of Event
    March 15, 2011
    Report Date
    March 15, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT HEADREST OF THE TROLLEY IS FAULTY. THE HEADREST WOULD WIGGLE FORWARDS AND BACKWARDS. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EYE SURGERY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1069 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA