BEUDAMED
    FDA Adverse Event Other Summary report: N

    QUINTON TREADMILL MEDTRACK R60

    MDR report key: 248538 · Received October 29, 1999

    Report

    Report Number
    248538
    Event Type
    Other
    Date Received
    October 29, 1999
    Date of Event
    October 27, 1999
    Report Date
    October 29, 1999
    Manufacturer
    QUINTON INSTRUMENT CO.
    Product Code
    IOL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NE, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    CLIENT WAS EXERCISING ON TREADMILL IN HOSP WELLNESS CTR. SHE WAS INCREASING SPEED FROM 3.0 TO 3.1 MPH - TREADMILL KEPT INCREASING IN SPEED AND SHE FELL. CONTUSIONS OF LEFT ELBOW AND KNEE. THIS CLIENT EXERCISES IN THE WELLNESS CTR ON A REGULAR BASIS AND HAS NOT HAD PREVIOUS DIFFICULTY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUINTON TREADMILL MEDTRACK R60 TREADMILL IOL QUINTON INSTRUMENT CO. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Other