BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RECOVERY AND TRANSPORT STRETCHERS HAUSTED

    MDR report key: 3904689 · Received June 2, 2014

    Report

    Report Number
    3904689
    Event Type
    Malfunction
    Date Received
    June 2, 2014
    Date of Event
    February 14, 2014
    Report Date
    June 2, 2014
    Manufacturer
    GF HEALTH PRODUCTS, INC.
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TN, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    FEMALE PATIENT WAS BEING TRANSPORTED TO ROOM WITH A HAUSTED STRETCHER. STRETCHER BRAKE WAS APPLIED WITH DIFFICULTY. WHILE PATIENT WAS SCOOTING FROM STRETCHER TO BED, STRETCHER BRAKE RELEASED AND BEGAN TO SEPARATE FROM THE BED. THE NURSE USED HER BODY WEIGHT TO KEEP STRETCHER IN PLACE. STAFF WAS ABLE TO SAFELY MOVE PATIENT TO BED WITHOUT ANY UNTOWARD EFFECTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    321809 RECOVERY AND TRANSPORT STRETCHERS HAUSTED STRETCHER INK GF HEALTH PRODUCTS, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 38 YR