PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Medical Systems
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging equipment and solutions.
Lower-risk recall
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications
What happened, in plain English
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging equipment and solutions. Read more at govinfonow.com/recall/459400-philips-medical-systems-nederland-b-v-philips-medical-systems.
Source Summary by GovInfoNow · govinfonow.com/recall/459400-philips-medical-systems-nederland-b-v-philips-medical-systems · Updated August 27, 2026 · FDA enforcement record: FDA #Z-2931-2026
Cite this page
“PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Medical Systems.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/459400-philips-medical-systems-nederland-b-v-philips-medical-systems. Based on FDA recall #Z-2931-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2931-2026%22&limit=1).
Why it’s dangerous
The company is a legitimate medical device manufacturer with no known security risks.
Who’s affected
All users of medical imaging equipment from Philips Medical Systems Netherlands B.V.
How to tell if you have this one
Check for updates and patches for medical imaging software from Philips Medical Systems.
- Brand
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.- Product
Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224- Category
Medical device
What to do — step by step
1
Verify the company's legitimacy through official channels.
2
Ensure that all medical imaging equipment is updated to the latest software versions.
3
Monitor for any security advisories from Philips Medical Systems.
How this recall unfolded
Recall timeline
FDA published this recall 34 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
Questions people ask
How can I ensure my medical imaging equipment is secure?
Regularly update your medical imaging software to the latest versions and follow the security best practices provided by Philips Medical Systems.
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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-2931-2026 (July 16, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2931-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 27, 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.