Health product recall

Philips Hemodynamic Application

Last updated

Summary

Product
Philips Hemodynamic Application
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Philips Hemodynamic Application

Not applicable.

002010

Issue

Philips has become aware of a potential issue with Philips Interventional Hemodynamic Application R1.2.X, R1.3.0 and R1.3.1, where synchronization of pressure wave data received from two devices, the Intellivue X3 and Functional Measurement Patient Interface Module (FM-PIM) may not be correct. There might be a delay of the FM-PIM data with respect to the Intellivue X3 data which is not constant in time. When this occurs, the calculation of measurements will be affected, specifically the IFR (Instantaneous Wave-Free Ratio) and FFR (Fractional Flow Reserve) values.

Recall Start Date: May 3, 2024

 

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Philips Medical Systems Nederland B.V.

Veenpluis 6, Best, Netherlands, 5684 PC

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75526

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