BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    7863712

    MDR report key: 7863712 · Received September 11, 2018

    Report

    Report Number
    7863712
    Event Type
    Malfunction
    Date Received
    September 11, 2018
    Date of Event
    August 20, 2018
    Report Date
    August 30, 2018
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MN
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    ARTERIAL LINE GIVING FALSE LOW HEMOGLOBIN READINGS WHICH POTENTIALLY IMPACTED THE AMOUNT OF TRANSFUSIONS PATIENTS GIVEN. ANESTHESIA SENT BLOOD DOWN TO LAB TO COMPARE READINGS AND THEY WERE MUCH DIFFERENT.

    Patients

    Seq Age Sex Outcome Treatment
    1 10585 DA