BEUDAMED
    FDA Adverse Event Other Summary report: N

    AMBU SPUR ADULT

    MDR report key: 346466 · Received August 9, 2001

    Report

    Report Number
    1220828-2001-00003
    Event Type
    Other
    Date Received
    August 9, 2001
    Report Date
    August 8, 2001
    Manufacturer
    AMBU, INC.
    Product Code
    BTM
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHILE BAGGING THE PT, RESPIRATORY PERSONNEL SHOW THE STAPLE PIN IN THE COMPRESSION BAG, STOP BAGGING AND USED ANOTHER CPR BAG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    35961 AMBU SPUR ADULT MANUAL RESUSCITATOR BTM AMBU, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other