BEUDAMED
    FDA Adverse Event Other Summary report: N

    OMI

    MDR report key: 359741 · Received October 26, 2001

    Report

    Report Number
    1525725-2001-00018
    Event Type
    Other
    Date Received
    October 26, 2001
    Date of Event
    August 8, 2001
    Report Date
    October 26, 2001
    Manufacturer
    OHIO MEDICAL INSTRUMENT CO.
    Product Code
    FPO
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    APPROXIMATELY 6 STAFF MEMBERS CUT HANDS AND/OR ARMS ON HANDRAIL OF BED BECAUSE CHROME IS PEELING OFF, LEAVING SHARP EDGES EXPOSED ALONG RAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    48238 OMI STRETCHER FPO OHIO MEDICAL INSTRUMENT CO. 545 *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other