BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GAS

    MDR report key: 327769 · Received April 16, 2001

    Report

    Report Number
    MW1021651
    Event Type
    Injury
    Date Received
    April 16, 2001
    Date of Event
    March 27, 1998
    Report Date
    April 16, 2001
    Manufacturer
    ALCON
    Product Code
    LPO
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT HAD KIDNEY TRANSPLANT WITH NITROUS OXIDE AS INDUCTION AGENT; HAD UNDERGONE VITRECTOMY 3 WEEKS PRIOR. BLINDNESS IN ONE EYE. ALCON HAS SENT BRACELETS TO BE PLACED ON PTS GETTING GAS BUBBLE INJECTIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    17264 GAS ISPAN PERFLOROPROPANE C3 F8 LPO ALCON * NOT DONE @ UCSD

    Patients

    Seq Age Sex Outcome Treatment
    1 19 YR Disability