PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Medical Systems
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging systems and equipment. They provide a wide range of products including MRI, CT, X-ray, and ultrasound systems. Their products are used in hospitals and clinics worldwide for diagnostic imaging and patient care.
Lower-risk recall
Firmware issue potentially leading to loss of geometry movements.
What happened, in plain English
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is a leading manufacturer of medical imaging systems and equipment. They provide a wide range of products including MRI, CT, X-ray, and ultrasound systems. Their products are used in hospitals and clinics worldwide for diagnostic imaging and patient care. Read more at govinfonow.com/recall/459447-philips-medical-systems-nederland-b-v-philips-medical-systems.
Source Summary by GovInfoNow · govinfonow.com/recall/459447-philips-medical-systems-nederland-b-v-philips-medical-systems · Updated August 27, 2026 · FDA enforcement record: FDA #Z-2928-2026
Cite this page
“PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Medical Systems.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/459447-philips-medical-systems-nederland-b-v-philips-medical-systems. Based on FDA recall #Z-2928-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2928-2026%22&limit=1).
Why it’s dangerous
This is a low-risk brand as it is a well-known manufacturer of medical imaging systems and equipment. The brand is used in hospitals and clinics worldwide for diagnostic imaging and patient care. There are no known security vulnerabilities associated with this brand.
Who’s affected
All users of medical imaging systems and equipment from Philips Medical Systems Netherlands B.V.
How to tell if you have this one
Ensure that the medical imaging systems and equipment are properly maintained and updated to the latest security patches. Check for any unauthorized access attempts or unusual activity on the systems.
- Brand
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.- Product
Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional- Category
Medical device
What to do — step by step
1
Verify the manufacturer's identity and ensure that the medical imaging systems are from a legitimate source.
2
Ensure that the medical imaging systems are properly maintained and updated to the latest security patches.
3
Check for any unauthorized access attempts or unusual activity on the systems.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Canada, Algeria, Argentina, Australia, Austria, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Czech Republic, Denmark,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 51 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.
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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-2928-2026 (June 29, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2928-2026 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.