BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIONVILLE

    MDR report key: 1628169 · Received March 5, 2010

    Report

    Report Number
    1628169
    Event Type
    Malfunction
    Date Received
    March 5, 2010
    Date of Event
    August 27, 2009
    Report Date
    August 27, 2009
    Manufacturer
    LIONVILLE SYSTEMS, INC
    Product Code
    BZN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MS, US

    Narratives

    Description of Event or Problem · 1

    STAFF REPORTED MED CART WOULD NOT HOLD A CHARGE. BIOMED CHECKED/REPLACED THE BATTERY. UNIT STILL WOULD NOT HOLD A CHARGE. BIOMED THEN PULLED THE CHARGING UNIT OUT OF THE MED CART AND FOUND THE QUICK DISCONNECT CONNECTOR THAT LEADS TO THE BATTERIES WAS BURNT. THE ONLY FUSE IN THE CIRCUIT, LOCATED BETWEEN THE BATTERY AND THE POWER SUPPLY WAS NOT BLOWN. BIOMED VOICED THE CONCERN THAT THE WAY THE CHARGER IS DESIGNED, A FIRE COULD OCCUR IN ITS CIRCUITRY WITHOUT EVER BLOWING THE FUSE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIONVILLE MEDICATION ACUTE CARE CART BZN LIONVILLE SYSTEMS, INC 800 SERIES *

    Patients

    Seq Age Sex Outcome Treatment
    1 *