Safety Alert for intellispace portal dx/hx/ex, intellispace portal ix, and intellispace portal lx spect

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Philips Healthcare.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2014-08-07
  • Event Date Posted
    2014-08-07
  • Event Country
  • Event Source
    DH
  • Event Source URL
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Medical device safety alert: philips healthcare intellispace portal dx/hx/ex, intellispace portal ix, and intellispace portal lx spect medical device manufacturer, philips healthcare, has issued a field safety notice (fsn) concerning its intellispace portal dx/hx/ex, intellispace portal ix, and intellispace portal lx spect (software versions: 5 and 6). the affected software versions include 5.0.0, 5.0.1, 5.0.2, 6.0.0, 6.0.1 and 6.0.2. there are four problems mentioned in the fsn: problem 1: when reopening a bookmark generated from processing a muga (multi-gated acquisition) scan within the nm cardiac application, the ejection fraction (ef) displayed should be the same as the ef originally displayed when the bookmark was first created. in some instances, the ef may be different. there is a risk of the patient receiving an incorrect treatment plan. problem 2: when processing using one of the following nm clinical applications: auto quant, emory cardiac toolbox, corridor4dm, or neuroq, the patient study presented to the reviewing physician within the application may be for a different patient than the one selected from the patient directory. there is risk of the patient receiving an incorrect treatment plan due to misdiagnosis. problem 3: while using the nm viewer application, an arrow annotation added to a display moves away from its original position if the viewer is subsequently maximized or if the image within the viewer is subsequently zoomed in or out. incorrect area indicator annotation results in an erroneous final nuclear medicine report, which may cause subsequent mistreatment. problem 4: while displaying pet images within ct viewer, the suv results displayed may be calculated with an suv method different from the one specified in system preferences. there is a risk of misdiagnosis if suv calculation method applied is not the method selected by the user. the manufacturer will install updated software versions 5.0.2.3 and 6.0.2.3 to correct the issue. service engineer will contact the customer for implementation of the software update on the affected systems. until the site’s software is updated, the manufacturer advises users to perform the workarounds mentioned in the fsn based upon the above problem descriptions. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 7 aug 2014.

Device

  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Philips Healthcare IntelliSpace Portal DX/HX/EX, IntelliSpace Portal IX, and IntelliSpace Portal LX SPECT
  • Manufacturer

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    DH