Use cautionMedical device recall · FDA · Published March 10, 2025
Philips X-Ray System Recall: Collimator Fall Risk
Philips recalls DXR System and DuraDiagnost Rel. 4 X-Ray systems with potential collimator fall risk due to incorrect installation. Affected units include specific serial numbers.
“Philips X-Ray System Recall: Collimator Fall Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52650-philips-x-ray-system-recall-collimator-fall-risk. Based on FDA recall #Z-1554-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1554-2025%22&limit=1).
Philips North America Llc recalled Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray Systems due to a potential collimator fall from incorrect installation, the FDA said on March 10, 2025.
How to tell if you have it
Brand: Philips
Product: Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System
The recall addresses the potential for the collimator to fall as a result of incorrect installation.
Context
GovInfoNow's records show Philips North America Llc has 129 other recalls on record since July 12, 2017. Other recent recalls of similar products include Accuray Cyberknife System Recall: Collimator May Fall During Treatment (June 16, 2026), GE Optima XR200amx Mobile Radiography System Recall: Column Safety Risk (June 5, 2026) and GE Optima XR240amx Mobile X-Ray System Recall: Column Safety Failure Risk (June 5, 2026).
How to tell if you have this one
Check for serial numbers SN170009, SN170010, SN180072, SN180020, 200037, SN160061, SN180075, 200089, SN180045, or SN160096 on the equipment. The recall covers specific models from Philips North America.
Brand
Philips
Product
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Worldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH, NY, OR, PA, TX, WI and the countries of Argentina, Australia, Canada, Chile, China, Germany, Hungary, India, Indonesia, Italy, Kenya, Mexico, Netherlands, New Zealand, Oman, Pakistan, Peru, Poland, Romania, Russian Federation, Slovenia, South Africa, Spain, Thailand, United Kingdom, Vietnam.
Verify the collimator is installed correctly to prevent falls.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 10 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH, NY, OR, PA, TX, WI and the countries of Argentina, Australia, Canada, Chile, China, Germany, Hungary, India, Indonesia, Italy, Kenya, Mexico, Netherlands, New…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alaska, Florida, Kansas, Mississippi, New Hampshire, New York, Oregon, Pennsylvania, Texas, Wisconsin.
Recall timeline
FDA published this recall 44 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1554-2025 (March 10, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1554-2025 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.