Philips recalls ProxiDiagnost N90-A radiography systems due to potential incorrect patient data display and security vulnerabilities in wireless detectors. Affected units have specific serial numbers and UDI codes.
Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patient s 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)
Philips is recalling its ProxiDiagnost N90-A multi-functional radiography systems because they may show previous patient images during new scans, risking incorrect patient data. There's also a security vulnerability in wireless detectors that could allow data export to removable media with physical access.
The system may display previous patient radiography images during new scans, causing incorrect patient data to appear. Wireless detectors have a security vulnerability that could let someone with physical access and specific knowledge modify and export data to USB drives.
Healthcare facilities using Philips ProxiDiagnost N90-A systems with specific serial numbers or UDI codes are affected. Medical staff handling these systems face the highest risk due to potential data errors and security issues.
Check for serial numbers listed in the recall notice (e.g., 10001064-10001168) or UDI codes (00884838085619, 00884838103221). The recall includes units sold in the US and other countries with specific serial numbers.
Review the list of affected serial numbers provided in the recall notice to confirm if your unit is included.
Philips recalls the ProxiDiagnost N90-A systems due to two issues: mixed images that could show previous patient data during new scans, and a security vulnerability in wireless detectors that might allow data export to removable media.
Check if your unit has serial numbers listed in the recall (e.g., 10001064-10001168) or UDI codes (00884838085619, 00884838103221). The recall includes specific units sold in the US and other countries.
The recall does not specify a remedy, so no action is required beyond checking if your unit is affected. Philips has not provided a fix or replacement.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1072-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1072-2024 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
