BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 1900130 · Received November 9, 2010

    Report

    Report Number
    1831750-2010-03620
    Event Type
    Injury
    Date Received
    November 9, 2010
    Date of Event
    October 12, 2010
    Report Date
    October 13, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV.
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    BASED ON THE REPORTED EVENT, THIS IS A CASE OF USER ERROR, HOWEVER, STRYKER MEDICAL HAS NOT YET COMPLETED AN EVAL OF THE DEVICE. INVESTIGATION IS UNDERWAY.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A NURSE HAS BEEN LIFTING THE BACK REST INCORRECTLY AND THAT ALTHOUGH SHE WAS ASKED TO USE TWO HANDS REPEATEDLY BY HOSPITAL STAFF, SHE CONTINUES TO USE ONLY ONE AND HAS NOW ALLEGEDLY INJURED HERSELF. IT WAS REPORTED THAT THE NURSE INJURED HER BACK WHILE LIFTING THE BACKREST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EYE SURGERY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MEDICAL DIV. 1089 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other