BEUDAMED
    FDA Adverse Event Other Summary report: N

    OMI

    MDR report key: 423879 · Received October 23, 2002

    Report

    Report Number
    1525725-2002-00038
    Event Type
    Other
    Date Received
    October 23, 2002
    Report Date
    September 18, 2002
    Manufacturer
    OHIO MEDICAL INSTRUMENT CO.
    Product Code
    INW
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT WAS ON STRETCHER LYING ON THEIR SIDE WITH THE SIDE RAILS UP AND LOCKED. THE PATIENT WAS REPOSITIONING THEMSELF AND LEANED AGAINST THE SIDERAIL. THE SIDERAIL DROPPED AND SO DID THE PATIENT LANDING ON THEIR HEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OMI STRETCHER INW OHIO MEDICAL INSTRUMENT CO. 550 *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other