BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AEQUITRON MEDICAL INC.

    MDR report key: 147038 · Received January 5, 1998

    Report

    Report Number
    147038
    Event Type
    Injury
    Date Received
    January 5, 1998
    Date of Event
    October 24, 1997
    Report Date
    October 31, 1997
    Manufacturer
    NELCOR PURITTAN-BENNETT
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MI, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    AFTER REPOSITIONING PT, HE COMPLAINS OF DIFFICULTY BREATHING, HIGH PRESSURE, LOW PRESSURE AND LOW POX ALARM GOING OFF. PT COMPLAINS OF DIFFICULTY EXHALING. PT WAS THEN DISCONNECTED AND BAGGED WITH COLOR RETURNING AND BECAME MORE ALERT. VENT WAS CHECKED BY RESPIRATORY THERAPY AND FUNCTIONING WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AEQUITRON MEDICAL INC. VENT CBK NELCOR PURITTAN-BENNETT LP10 *

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR Life Threatening| O| R