BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MIDAS REX I MO

    MDR report key: 318366 · Received February 27, 2001

    Report

    Report Number
    1625507-2001-00397
    Event Type
    Malfunction
    Date Received
    February 27, 2001
    Report Date
    December 15, 2000
    Manufacturer
    MEDTRONIC MIDAS REX
    Product Code
    HBB
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    DURING CASE, HOSE STARTED HISSING AND BLEW OUT HOT AIR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    7914 MIDAS REX I MO PNEUMATIC SURGICAL DRILL HBB MEDTRONIC MIDAS REX NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *