Events

Recall of ULTRAVIEW 1700 MONITOR

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by DATEX-OHMEDA (CANADA) INC..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    23596
  • Event Risk Class
    II
  • Event Initiated Date
    2004-05-17
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    Manufacturer has reports of an anomaly that causes the telemetry channels to drop-off the display.

Device

ULTRAVIEW 1700 MONITOR
  • Model / Serial
    Model Catalog: 90387 (Lot serial: S/N 387-3XXXXX OR HIGHER); Model Catalog: 90385 (Lot serial: S/N 385-3XXXXX OR HIGHER)
  • Product Description
    CENTRAL STATION MONITOR
  • Manufacturer
    DATEX-OHMEDA (CANADA) INC.

Manufacturer

DATEX-OHMEDA (CANADA) INC.
  • Manufacturer Address
    MISSISSAUGA
  • Source
    HC