BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PURITAN BENNET 7200 SERIES

    MDR report key: 458246 · Received May 1, 2003

    Report

    Report Number
    MW1028326
    Event Type
    Injury
    Date Received
    May 1, 2003
    Date of Event
    April 2, 2003
    Report Date
    May 1, 2003
    Manufacturer
    TYCO HEALTH CARE, INC./ PURITAN BENNET
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT. IN CCU, DIAGNOSIS, CHEST PAIN R/O MI. NEAR RESP. ARREST, INTUBATED AND ON VENT. VENT MALFUNCTIONED VS FAILURE. PT. REMOVED FROM VENT, AMBU BAGGED, AND VENT EXCHANGED. O2 SATS REMAINED INTACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PURITAN BENNET 7200 SERIES VENTILATOR CBK TYCO HEALTH CARE, INC./ PURITAN BENNET PB 7200 *

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Life Threatening| R