BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FLEXICAIR MC3

    MDR report key: 452186 · Received April 1, 2003

    Report

    Report Number
    1045510-2003-00008
    Event Type
    Malfunction
    Date Received
    April 1, 2003
    Date of Event
    March 8, 2003
    Report Date
    April 1, 2003
    Manufacturer
    HILL-ROM MANUFACTURING, INC.
    Product Code
    IOQ
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ALLEGATION THAT NURSE HURT THEIR BACK WHILE REPOSITIONING PATIENT DUE TO PROBLEM WITH RUBBER MISSING ON CASTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLEXICAIR MC3 LOW AIRLOSS THERAPY IOQ HILL-ROM MANUFACTURING, INC. M4000 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other