BEUDAMED
    FDA Adverse Event Summary report: N

    HBO MONOPLACE CHAMBER STRETCHER

    MDR report key: 2771571 · Received August 30, 2012

    Report

    Report Number
    2771571
    Date Received
    August 30, 2012
    Date of Event
    July 27, 2012
    Report Date
    August 30, 2012
    Manufacturer
    SECHRIST INDUSTRIES
    Product Code
    FPO
    Report Source
    User Facility report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    AFTER PATIENT COMPLETED HYPERBARIC OXYGEN TREATMENT, THE GURNEY WAS ATTACHED TO THE HBO CHAMBER AND THEN THE STRETCHER WITH PATIENT WAS REMOVED AND LOCKED ONTO GURNEY. THE ENTIRE UNIT WAS MOVED TO THE PATIENT CHANGING AREA IN THE HBO TREATMENT ROOM. WHEELS WERE THEN LOCKED AND UNIT ELEVATED TO ALLOW IT TO BE LOWERED FOR PATIENT TO TRANSFER OFF. THE STRETCHER WAS LOWERED TO ALLOW PATIENT TO TRANSFER OFF. HBO TECHNICIAN MOVED TO SIDE TO LOWER SIDERAIL. THE PATIENT BEGAN TO SIT UP AND MOVE TOWARD THE FOOT OF THE UNIT. THE STRETCHER PORTION TILTED DOWN TOWARDS THE FOOT END AND SLED UNTIL THE FOOT END OF THE STRETCHER HIT THE FLOOR. THE PATIENT SLID TOWARD THE FOOT OF THE UNIT BUT DID NOT FALL TO THE FLOOR. INITIALLY, PATIENT REPORTED NO DISCOMFORT OR INJURY.======================MANUFACTURER RESPONSE FOR HBO MONOPLACE CHAMBER STRETCHER, SECHRIST (PER SITE REPORTER).======================RESPONDED AND ATTEMPTED TO DETERMINE IF A PRODUCT MALFUNCTION OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HBO MONOPLACE CHAMBER STRETCHER STRETCHER, HYBERBARIC FPO SECHRIST INDUSTRIES 21483F *

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR