ProxiDiagnost N90 706110Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838103221), received between Jun 21, 2024 and Jun 21, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Fell” (1 report).

5 FDA recall records name this device's identifier, 5 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Oct 1, 2025Class IIOpen, Classified

   Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

   Z-0461-2026 · Root cause: Device Design · Recall details · FDA record ↗

2. Dec 15, 2023Class IIOpen, Classified

   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)

   Z-1072-2024 · Root cause: Software design · Recall details · FDA record ↗

3. Sep 21, 2023Class IIOpen, Classified

   Potential for units suspended on the ceiling to fail and fall.

   Z-0280-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

4. Oct 21, 2022Class IIOpen, Classified

   Potential table stop due to a broken tabletop cable: On the ProxiDiagnost N90 table there is a cable located under the tabletop that is covered by a plastic sleeve which can crack and damage the cable. If the tabletop cable breaks, the user may not be able to initiate table tilting movements or braking

   Z-1477-2023 · Root cause: Component design/selection · Recall details · FDA record ↗

5. Oct 21, 2021Class IIOpen, Classified

   If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.

   Z-1356-2023 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 21, 2024Use of Device Problem; Device Fell; Use of Device Problem; Device Fell

  IT WAS REPORTED THAT THERE WAS DAMAGE TO THE DETECTOR (SKYPLATE) WITH ARTIFACTS. IT WAS UNABLE TO CONNECT PORTABLE SKYPLATE DETECTOR TO THE SYSTEM. THERE WAS NO HARM TO PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19583462 ↗