Lower riskMedical device recall · FDA · Published January 2, 2024
Philips Azurion X-ray Systems Recall: Disk Bay May Cause Procedure Delays
Philips recalls Azurion Interventional Fluoroscopic X-ray Systems with specific disk bay models due to potential system failure during procedures. Affected units include Azurion 3 M12, M15, 5 M20, and 7 B12/B20/M12/M20 models with listed serial numbers.
Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
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Contact the company
📍Recalling firmPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Veenpluis 4-6 · Best, Netherlands
✎ GovInfoNow plain-language explainer
Philips is recalling specific models of Azurion Interventional Fluoroscopic X-ray Systems because the disk bay may not function properly, which could delay medical procedures. This issue affects certain versions of the system used in hospitals and clinics. Read more at govinfonow.com/recall/56434-philips-azurion-x-ray-systems-recall-disk-bay-may-cause.
“Philips Azurion X-ray Systems Recall: Disk Bay May Cause Procedure Delays.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/56434-philips-azurion-x-ray-systems-recall-disk-bay-may-cause. Based on FDA recall #Z-1152-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1152-2024%22&limit=1).
The FDA announced on Jan. 2, 2024, that Philips Medical Systems Nederland B.V. is recalling Philips Azurion Interventional Fluoroscopic X-ray Systems due to a Disk Bay hazard. The agency stated the component may fail, causing system shutdowns and procedure delays.
How to tell if you have it
Brand: Philips
Product: Azurion Interventional Fluoroscopic X-ray Systems
Affected PCs: XRay PC, Suite PC, FlexViewing PC
Azurion 3 M12 (722063, 722221)
Azurion 3 M15 (722064, 722222)
Azurion 5 M20 (722228)
Azurion 7 B12 (722067, 722225)
Azurion 7 B20 (722068, 722226)
Azurion 7 M12 (722078, 722223)
Azurion 7 M20 (722079, 722224)
The hazard
According to the FDA, the Disk Bay of the PC component may not perform as intended. The system may stop functioning and imaging may not be possible, resulting in delay of procedure.
Context
GovInfoNow's records show Philips Medical Systems Nederland B.V. has 58 other recalls on record since May 26, 2021. Other recent recalls of similar products include Philips Azurion R3.0 X-ray System Recall: Missing SSD Spacer Risk (Oct. 27, 2025), Philips Achieva 3.0T MRI Recalled: Software Issue May Terminate Scans (Aug. 21, 2026), and Philips Brilliance CT 64 Medical Scanner Recall: Unintended Radiation Risk (Aug. 7, 2026).
How to tell if you have this one
Check if your system is listed in the affected models: Azurion 3 M12, M15, 5 M20, or 7 B12/B20/M12/M20 with specific serial numbers provided in the recall notice.
Brand
Philips
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 Distribution: US nationwide including states of: AL, AK, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV, & WY; and OUS (International) to countries of: Afghanistan, Albania, Algeria, Argentina, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Fiji, Finland, France, French Polynesia, Gabon, Georgia, Germany, Ghana, Greece, Guadeloupe, Guinea, Honduras, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nicaragua, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Papua New Guinea, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russian Federation, Saudia Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Tanzania, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, and Yemen.
Identify your Philips Azurion system model and serial number to confirm if it's affected by this recall.
Contact Philips Support
Reach out to Philips customer support for assistance with the recall process if your system is listed.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 48 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide Distribution: US nationwide including states of: AL, AK, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 57 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-1152-2024 (January 2, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1152-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.