BEUDAMED
    FDA Adverse Event Other Summary report: N

    AIRLIFE ADULT MANUAL RESUSCITATOR

    MDR report key: 553261 · Received September 21, 2004

    Report

    Report Number
    553261
    Event Type
    Other
    Date Received
    September 21, 2004
    Date of Event
    September 7, 2004
    Report Date
    September 21, 2004
    Manufacturer
    CARDINAL HEALTH
    Product Code
    BTM
    Report Source
    User Facility report
    Reporter Location
    DC, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    WHEN USING THE RESUSCITATOR, THE INSIDES "STICK TOGETHER" WHEN COMPRESSED DURING VENTILATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AIRLIFE ADULT MANUAL RESUSCITATOR AMBU BAG BTM CARDINAL HEALTH * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *