BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9610816-2010-00527

    MDR report key: 1850075 · Received September 28, 2010

    Report

    Report Number
    9610816-2010-00527
    Event Type
    Malfunction
    Date Received
    September 28, 2010
    Report Date
    August 5, 2010
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    HFM
    PMA / PMN Number
    UNK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE CUSTOMER REPORTED THAT THERE WAS A FAILURE TO ALARM. NO PT HARM WAS REPORTED. PHILIPS IS IN THE PROCESS OF OBTAINING ADDITIONAL INFO CONCERNING THIS EVENT AND THE COMPLAINT IS STILL UNDER INVESTIGATION. A FINAL REPORT WILL BE SUBMITTED ONCE THE INVESTIGATION IS COMPLETED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THERE WAS A FAILURE TO ALARM. NO PT HARM WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HFM PHILIPS MEDICAL SYSTEMS M1383D

    Patients

    Seq Age Sex Outcome Treatment
    1