Lower riskMedical device recall · FDA · Published December 15, 2023
Philips ProxiDiagnost R/F System Recall: Mixed Images and Security Vulnerability
Philips recalls ProxiDiagnost upgrade A Multi-functional Radiography and Fluoroscopy systems due to potential incorrect patient data display and security vulnerabilities in wireless detectors.
Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patients radiography (RAD) images when starting the next patient scan while the previous patient image export is still processing. If the issue occurs, there is a potential for incorrect patient data to be displayed in the image. Issue 2: Detector Access point: Security vulnerability specific to the Wireless Portable Detector configuration items in Philips Support Connect (PSC). Due to this vulnerability it is possible, with physical access to the system and knowledge of specific settings, to modify and export data to removable media (example: USB)
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Contact the company
📍Recalling firmPhilips North America222 Jacobs St · Cambridge, MA 02141-2296
✎ GovInfoNow plain-language explainer
Philips is recalling its ProxiDiagnost upgrade A Multi-functional Radiography and Fluoroscopy systems because they may display previous patient images during new scans, risking incorrect patient data. The systems also have a security vulnerability that could allow data export to removable media if physically accessed. Read more at govinfonow.com/recall/56551-philips-proxidiagnost-r-f-system-recall-mixed-images-and-security.
“Philips ProxiDiagnost R/F System Recall: Mixed Images and Security Vulnerability.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56551-philips-proxidiagnost-r-f-system-recall-mixed-images-and-security. Based on FDA recall #Z-1073-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1073-2024%22&limit=1).
Philips North America recalled the ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system on Dec. 15, 2023, according to the FDA. The device may display mixed images or have a security vulnerability allowing unauthorized data export.
How to tell if you have it
Brand: Philips
Product: ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
The Radio Fluoroscopy viewer may display a previous patient's radiography images when starting the next scan, potentially showing incorrect patient data. Additionally, a security vulnerability in the Wireless Portable Detector configuration allows modification and export of data to removable media with physical access and specific settings knowledge.
Context
GovInfoNow's records show Philips North America has 30 other recalls on record since 2020-12-24. Recent brand recalls include the Ingenia Elition S and Ingenia Elition X (2026-08-28), Patient Information Center iX Software freezes (2026-07-31), and MR 7700 MRE Device stiffness errors (2026-04-14). Other recent recalls of similar products include Philips Azurion X-Ray System Recall: Unauthorized Hard Drive Risk (2026-06-17), Philips Allura Xper Systems: Potential Loss of Imaging Functionality Due to Unauthorized Hard Drives (2026-06-17), and Philips Brilliance CT 64 Medical Scanner Recall: Unintended Radiation Risk (2026-08-07).
How to tell if you have this one
Check for serial numbers starting with US: 4 5 6 7 8 9 11 12 13 14 17 18 61 692222229, 692222254, or 692222263. The system is sold under the Philips ProxiDiagnost upgrade A Multi-functional Radiography and Fluoroscopy (R/F) name.
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
Nationwide Foreign: Australia Germany India Italy Malaysia Panama Thailand
ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150; UDI: N/A Serial Numbers US: 4 5 6 7 8 9 11 12 13 14 17 18 61 692222229 692222254 692222263 Serial Numbers OUS: 53 56 65 692222227
20 units: 16 units US; 4 units OUS
Based on the official FDA remedy
What to do — step by step
Check Serial Numbers
Verify your system's serial number starts with US: 4 5 6 7 8 9 11 12 13 14 17 18 61 692222229, 692222254, or 692222263.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Nationwide Foreign: Australia Germany India Italy Malaysia Panama Thailand” 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 2 months 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-1073-2024 (December 15, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1073-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.