BEUDAMED
    FDA Adverse Event Other Summary report: N

    OXICLIQ MODEL N SENSOR

    MDR report key: 231011 · Received July 1, 1999

    Report

    Report Number
    231011
    Event Type
    Other
    Date Received
    July 1, 1999
    Date of Event
    June 16, 1999
    Report Date
    June 28, 1999
    Manufacturer
    MALLINCKRODT
    Product Code
    DQA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CT, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    SKIN REDNESS, PEELING AT SITE OF O2 SAT MONITOR PROBE. POSSIBLE PRESSURE NECROSIS OR POSSIBLE SUPERFICIAL SKIN BURN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OXICLIQ MODEL N SENSOR O2 SAT MONITOR DQA MALLINCKRODT OXICLIQ N *

    Patients

    Seq Age Sex Outcome Treatment
    1 2 YR Other