BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SEIMENS

    MDR report key: 4017960 · Received August 9, 2014

    Report

    Report Number
    4017960
    Event Type
    Injury
    Date Received
    August 9, 2014
    Date of Event
    July 31, 2014
    Report Date
    August 6, 2014
    Manufacturer
    SIEMENS CORP
    Product Code
    LNH
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT WAS UNDERGOING AN MRI OF THE BRACHIAL PLEXUS. WHEN PREPARING THE PT FOR THE NEXT PORTION OF THE EXAM, IT WAS NOTED THAT SHE HAD DEVELOPED BLISTERING TO THE LATERAL PORTION OF HER UPPER ARM. THE PT WAS SENT TO THE EMERGENCY DEPT, WHERE SHE WAS DIAGNOSED WITH A SECOND DEGREE BURN. SHE WAS TREATED WITH ANALGESICS AND TOPICAL BURN OINTMENT. THE PT'S SKIN HAD WHAT WAS DESCRIBED AS A "GLITTERY LOOK" TO IT, POSSIBLY FROM THE PRESENCE OF LOTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    473641 SEIMENS AERA MRI MACHINE LNH SIEMENS CORP

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Other