BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BARIATRIC BED

    MDR report key: 10436113 · Received August 21, 2020

    Report

    Report Number
    10436113
    Event Type
    Malfunction
    Date Received
    August 21, 2020
    Date of Event
    July 4, 2020
    Report Date
    August 12, 2020
    Manufacturer
    KREG MEDICAL INC.
    Product Code
    OSI
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    BED UNABLE TO MOVE TO LOW POSITION. CORD WAS BROKEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    900908 BARIATRIC BED OSI KREG MEDICAL INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 27010 DA