BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 242522 · Received September 28, 1999

    Report

    Report Number
    242522
    Event Type
    Other
    Date Received
    September 28, 1999
    Date of Event
    September 20, 1999
    Report Date
    September 20, 1999
    Manufacturer
    HAMILTON INDUSTIRES GORMAN-RUPP AMERICAN PHARMASTAL CO.
    Product Code
    DWJ
    Report Source
    User Facility report
    Reporter Location
    NY, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    AS PER THE ANESTHESIOLOGIST THE MACHINE WAS SET AT 38 DEGREE CELSIUS - BUT SHE NOTED THE DIAL READ 45 DEGREES CELSIUS. THIS WAS NOTED AFTER PT WAS TRANSFERRED TO THE STRETCHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * HYPERTHERMIA BLANKET DWJ HAMILTON INDUSTIRES GORMAN-RUPP AMERICAN PHARMASTAL CO. RK-300 *

    Patients

    Seq Age Sex Outcome Treatment
    1 42 YR Other