Smartperfusion and 2D perfusion
Last updated
Summary
Product
Smartperfusion and 2D perfusion
Issue
Medical devices - Performance
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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