BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MIDAS REX I MO

    MDR report key: 294807 · Received September 7, 2000

    Report

    Report Number
    1625507-2000-00013
    Event Type
    Malfunction
    Date Received
    September 7, 2000
    Date of Event
    December 15, 1999
    Report Date
    September 7, 2000
    Manufacturer
    MEDTRONIC MIDAS REX
    Product Code
    HBB
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    OIL LEAKED THROUGH HANDPIECE ONTO FIELD. NO PT INTERVENTION REQUIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MIDAS REX I MO PNEUMATIC DRILL SYSTEM HBB MEDTRONIC MIDAS REX NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *