BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PULSE OXIMETER

    MDR report key: 12152 · Received March 21, 1994

    Report

    Report Number
    MW1001173
    Event Type
    Injury
    Date Received
    March 21, 1994
    Date of Event
    February 9, 1994
    Report Date
    March 15, 1994
    Manufacturer
    NONIN MEDICAL, INC.
    Product Code
    DQA
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Narratives

    Description of Event or Problem · 1

    PT RECEIVED A RADIO FREQUENCY BURN ON HER LEFT INDEX FINGER DURING AN MRI SCAN OF THE LUMBAR SPINE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PULSE OXIMETER PULSE OXIMETER DQA NONIN MEDICAL, INC. 8604D

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR Required Intervention