Health product recall

Smartperfusion and 2D perfusion

Last updated

Summary

Product
Smartperfusion and 2D perfusion
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 catalogue number

Smartperfusion

More than 10 numbers, contact manufacturer.

RELEASE 1.0

2D Perfusion

More than 10 numbers, contact manufacturer.

001008

Issue

Philips has identified through an internal investigation that Smartperfusion and 2D perfusion have technical issues related to the way the perfusion signal is generated and processed, which may lead to inaccurate presentations of time density curves and images.

Recall start date: February 22, 2023

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-73010

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