BEUDAMED
    FDA Adverse Event Summary report: N

    TEMPERATURE PROBE

    MDR report key: 22956 · Received June 28, 1995

    Report

    Report Number
    MW1006371
    Date Received
    June 28, 1995
    Date of Event
    May 24, 1995
    Report Date
    June 13, 1995
    Manufacturer
    YELLOW SPRINGS INSTRUMENT CO., INC.
    Product Code
    FLL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT STATUS DETERIORATION. RETURNED FROM INTERMEDIATE TO ACUTE ICU. FOUND BLEEDING ARTERIAL EROSION WHEN RECTAL PROBE REMOVED. AREA REQUIRED PHYSICIAN SUTURING. UNABLE TO ACCURATELY DETERMINE THE LENGTH OF PROBE DURATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TEMPERATURE PROBE TEMPERATURE PROBE FLL YELLOW SPRINGS INSTRUMENT CO., INC. 4400 NI

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR