BEUDAMED
    FDA Adverse Event Injury Summary report: N

    KINAIR III

    MDR report key: 518446 · Received March 16, 2004

    Report

    Report Number
    MW1031552
    Event Type
    Injury
    Date Received
    March 16, 2004
    Date of Event
    January 17, 2004
    Report Date
    March 8, 2004
    Manufacturer
    KINETIC CONCEPTS INC.
    Product Code
    IOQ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    OCCURRENCE: ENTRAPMENT. ROUND NURSE HEARD PT CALL OUT FOR HELP. FOUND PT CAUGHT BETWEEN KINAIR III BED SIDERAILS AND THE MATTRESS. ONLY PT'S FEET WERE ON THE FLOOR. PT WAS HELPED DOWN TO THE FLOOR WITH THE ASSISTANCE OF OTHER STAFF. ONLY INJURY WAS MINOR ABRASION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KINAIR III AIR-FLOTATION, LOW AIR ALOSS SUPPORT SYSTEM IOQ KINETIC CONCEPTS INC. 0556968 *

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR