BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OMNICELL I.V.STATION ONCO

    MDR report key: 10332186 · Received July 28, 2020

    Report

    Report Number
    3011278888-2020-00014
    Event Type
    Malfunction
    Date Received
    July 28, 2020
    Date of Event
    July 9, 2020
    Report Date
    May 20, 2021
    Manufacturer
    OMNICELL, INC.
    Product Code
    NEP
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    AS OF (B)(6) 2020, THE ESTABLISHMENT REGISTRATION AND LISTING FOR THIS DEVICE WAS UPDATED TO OMNICELL, INC. FROM AESYNT, INC, WHICH WAS NOT REFLECTED IN THE ORIGINAL REPORT SUBMISSION. THEREFORE, THIS REPORT IS A CORRECTION TO THE MANUFACTURER LISTED IN SECTIONS D3 AND G1.

    Description of Event or Problem · 1

    ON (B)(6) 2020 A SPILL INVOLVING A CHEMOTHERAPY DRUG PREPARATION OCCURRED INSIDE THE I.V. STATION ONCO DEVICE. THE SPILL OCCURRED DURING VIAL WITHDRAWAL OR INJECTION INTO THE BAG AND MAY BE ATTRIBUTED TO CONSUMABLES. THE ISSUE WAS NOT ABLE TO BE REPRODUCED. NO DEVICE MODIFICATIONS WERE MADE AND THE ISSUE HAS NOT RECURRED. THE SPILL WAS IDENTIFIED AND SUBSEQUENTLY CLEANED BY THE USER. THERE IS NO ADVERSE PATIENT EFFECT RELATED TO THIS DRUG SPILL WITHIN THE DEVICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    797726 OMNICELL I.V.STATION ONCO PHARMACY COMPOUNDING DEVICE NEP OMNICELL, INC. I.V. STATION ONCO

    Patients

    Seq Age Sex Outcome Treatment
    1 Other