BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CODE ALERT SYSTEM & BRACELET #24

    MDR report key: 209388 · Received February 10, 1999

    Report

    Report Number
    209388
    Event Type
    Malfunction
    Date Received
    February 10, 1999
    Date of Event
    August 22, 1998
    Report Date
    September 28, 1998
    Manufacturer
    R.F. TECHNOLOGIES, INC.
    Product Code
    KMI
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    TWO-DAY-OLD BABY LEFT THE HOSP WITH CODE ALERT BAND #24 ON. CODE ALERT SYSTEM DID NOT ALARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CODE ALERT SYSTEM & BRACELET #24 TRANSMITTER KMI R.F. TECHNOLOGIES, INC. CA 9400 *

    Patients

    Seq Age Sex Outcome Treatment
    1 2 DAY Other