Events

Recall of PANORAMA PATIENT MONITORING NETWORK - TOWER

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by MINDRAY DS USA 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
    33615
  • Event Risk Class
    III
  • Event Initiated Date
    2016-03-31
  • 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
    The time on the panorama central station including the workstation viewstation and the egateway will revert to the year 2000 when daylight savings time (dst) occurs or when the device is manually changed to 2016 or when the time is manually changed when the year is set to 2016.

Device

PANORAMA PATIENT MONITORING NETWORK - TOWER
  • Model / Serial
    Model Catalog: 0998-00-0700-01 (Lot serial: software v8.9 or higher); Model Catalog: 0998-00-0705-01 (Lot serial: software v8.9 or higher)
  • Product Description
    Panorama Central Station
  • Manufacturer
    MINDRAY DS USA INC.

Manufacturer

MINDRAY DS USA INC.