Philips Azurion 7 M20 FlexArm System Software Recall: Connectivity Loss Risk
Philips recalls Azurion 7 M20 FlexArm systems with specific Maquet Magnus Table software versions due to potential connectivity loss between components. Affected units have unique serial numbers and system codes.
Lower-risk recall
Loss of connectivity between the FlexArm and the Table due to a software issue.
Contact the company
What happened, in plain English
Philips is recalling Azurion 7 M20 FlexArm systems paired with Maquet Magnus Tables that have specific software versions. This recall is due to a software issue that could cause loss of connectivity between the FlexArm and Table, potentially disrupting medical procedures. Read more at govinfonow.com/recall/56585-philips-azurion-7-m20-flexarm-system-software-recall-connectivity-loss.
Source Summary by GovInfoNow · govinfonow.com/recall/56585-philips-azurion-7-m20-flexarm-system-software-recall-connectivity-loss · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0860-2024
Cite this page
“Philips Azurion 7 M20 FlexArm System Software Recall: Connectivity Loss Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/56585-philips-azurion-7-m20-flexarm-system-software-recall-connectivity-loss. Based on FDA recall #Z-0860-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0860-2024%22&limit=1).
Why it’s dangerous
The software issue causes the FlexArm and Table to lose connectivity, which could interrupt medical procedures. This is a technical malfunction that might require reconfiguration but does not pose an immediate physical danger to users.
Who’s affected
Healthcare facilities using the Azurion 7 M20 FlexArm system with Maquet Magnus Table software versions R2.x and 05.02.12 are most at risk. Medical staff and patients using these systems may experience temporary disruptions during procedures.
How to tell if you have this one
Check for system code 722079 or 722224, and serial numbers listed in the recall notice. The affected units have specific software versions: FlexArm R2.x and Maquet Magnus Table 05.02.12.
- Brand
Philips- Category
Medical device
What to do — step by step
Check Software Versions
Verify the FlexArm software version is R2.x and the Maquet Magnus Table software version is 05.02.12.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 6 states.
FDA distribution: “Worldwide - US Nationwide distribution in the states of CO, FL, IL, MS, NV and TX. The country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Colorado, Florida, Illinois, Mississippi, Nevada, Texas.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0860-2024 (December 8, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0860-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.