Health product recall

Azurion 7 M20

Last updated

Summary

Product
Azurion 7 M20
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

Azurion 7 M20

All lots.

722 224

Issue

Philips has become aware of a potential safety issue with the Azurion 7 M20 Flexarm System ("flexarm") with a Maquet Magnus Table with software versions 05.02.12 and 05.02.15 ("table"). Due to a communication issue between the flexarm and the table, motorized movements of the table and/or the flexarm may be lost. A representative of Getinge (manufacturer of the Maquet Magnus Table) will arrange a site visit to return the software of your table to version 05.02.12. After this change, your system will be subject to the medical device recall letter (HS23039R/2023-IGT-BST-020).

Recall start date: December 13, 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-74843

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe