Health product recall

Philips Azurion and Allura Systems

Last updated

Summary

Product
Philips Azurion and Allura Systems
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 numbe

Model or catalog numbe

Not applicable.

722 224
722 079

Allura Xper FD10 (Product Of AlluraClarity Family)

Not applicable.

722026

Allura Xper FD10

Not applicable.

001443

Allura Xper FD20 Or Table (Part Of AlluraClarity Family)

Not applicable.

722035

Allura Xper FD20 (Product Of AlluraClarity Family)

Not applicable.

722028

Issue

Due to the forces applied during the movement of the C-arc of the Azurion and Allura systems, the bolts supporting the flexmove carriage may become loose and/or break, and cracks may appear in the flexmove carriage.

Recall start date : June 12, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
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-73869

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