BEUDAMED
    FDA Adverse Event Summary report: N

    GEMINI 20 N/NV TUBING

    MDR report key: 13240 · Received May 13, 1994

    Report

    Report Number
    MW1001981
    Date Received
    May 13, 1994
    Date of Event
    May 7, 1994
    Report Date
    May 8, 1994
    Manufacturer
    IMED CORP.
    Product Code
    FPA
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    WHEN INSERTING TUBING SPIKE INTO BOTTLE OF IV FLUID, RPTR TURNED BOTTLE UPRIGHT TO PURGE TUBING. IV FLUID LEAKED FROM AREA WHERE SLIDE CLAMP FITS INTO PUMP, LEAKING IV FLUID EVERYWHERE. THE FLUID WAS HYPERALIMENTATION BUT IT VERY WELL COULD HAVE BEEN CHEMOTHERAPY OR OTHER TOXIC FLUID.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GEMINI 20 N/NV TUBING FPA IMED CORP. 94K031 03

    Patients

    Seq Age Sex Outcome Treatment
    1 *