Official recall record

Azurion 7 M20 (ref 74843)

Health Canada — Medical Devices · 2024-01-04 · CanadaType II

Issuing authority: Health Canada — Medical Devices
Published: 2024-01-04
Country of alert: Canada
Alert level: Type II
Alert type: recall

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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