BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PHILIPS MP50 M3001A

    MDR report key: 2213782 · Received August 16, 2007

    Report

    Report Number
    MW5021730
    Event Type
    Injury
    Date Received
    August 16, 2007
    Date of Event
    August 1, 2007
    Report Date
    August 15, 2007
    Manufacturer
    PHILIPS GCX CORP.
    Product Code
    DQA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT WAS BEING MONITORED WHILE UNDERGOING THORACOSCOPY, IN SURGERY. UNABLE TO PALPATE WRIST PULSE (WHEN ATTEMPTING TO DRAW BLOOD FROM A-LINE). BLOOD GAS DRAWN PCO2 67, PO2 47, SAO2 71%. NOT CONSISTENT WITH PULSE OX MONITOR. PROBE PLACED ON SAME HAND AS PHILIPS MONITOR 70%. PHILIPS PROBE REPLACED ON ANOTHER FINGER-SAME HAND - NOW READS 71%. CONVERTED BACK TO 2 LUNG VENT. SAO2 ON BOTH OX UPTO 99-100%.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PHILIPS MP50 M3001A PHILIPS MODULE M3001A DQA PHILIPS GCX CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR