ProxiDiagnost N90Recalls & reported problems across all models
Philips Medical Systems DMC GmbH · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
5 open recalls name at least one ProxiDiagnost N90 model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 5
We found 2 models of ProxiDiagnost N90 by Philips Medical Systems DMC GmbH in the FDA's device registry (GUDID). Together they are named in 7 adverse event reports in the FDA's MAUDE database, received between Dec 17, 2020 and Apr 22, 2026 — classified as 1 injury, 6 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
5 FDA recall records name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
ProxiDiagnost N90 recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Oct 1, 2025Open, 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 ↗
- Dec 15, 2023Open, 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 · names 2 of these models · Recall details · FDA record ↗
- Sep 21, 2023Open, Classified
Potential for units suspended on the ceiling to fail and fall.
Z-0280-2024 · Root cause: Under Investigation by firm · names 2 of these models · Recall details · FDA record ↗
- Oct 21, 2022Open, 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 · names 2 of these models · Recall details · FDA record ↗
- Oct 21, 2021Open, 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 · names 2 of these models · Recall details · FDA record ↗
Most reported ProxiDiagnost N90 problems
Device problems
- Detachment of Device or Device Component1
- Device Fell1
- Electrical /Electronic Property Problem1
- Flare or Flash1
- Mechanical Jam1
- Misassembled During Installation1
- Radiation Output Problem1
- Smoking1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Muscle/Tendon Damage1
- No Patient Involvement1
ProxiDiagnost N90 models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ProxiDiagnost N90 706110System, X-Ray, Fluoroscopic, Image-Intensified5 recalls1 report
- ProxiDiagnost N90 706100System, x-ray, fluoroscopic, image-intensified4 recalls6 reports
Recent ProxiDiagnost N90 adverse event reports
The 7 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionApr 22, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT THE PIECE OF THE FOOTBOARD WAS MISSING, RESULTING IN EXPOSED PARTS AND A POTENTIAL SAFETY CONCERN. THE DEVICE WAS OUTSIDE OF USE AND THERE WAS NO HARM TO THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24956411 ↗InjuryFeb 17, 2026Mechanical Jam
IT WAS REPORTED THAT THE WALKING MECHANISMS LOCK, AND WHEN MOVING FROM ONE SIDE OF THE ROOM TO ANOTHER, THE BUTTON CAN BE PUSHED TO MOVE FROM SIDE TO SIDE. WHEN PULLING IT ACROSS THE ROOM, IT JERKED THE STAFF'S ARM, CAUSING SHOULDER DAMAGE. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT HARM.
Patient problems: Muscle/Tendon Damage
MAUDE report 24373816 ↗MalfunctionJun 18, 2025Electrical /Electronic Property Problem; Smoking; Electrical /Electronic Property Problem; Smoking
IT WAS REPORTED THAT ELECTRICAL PART IN M-CABINET BURNED UP. THE USE OF DEVICE WAS UNKNOWN AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22269657 ↗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 ↗MalfunctionMar 22, 2023Misassembled During Installation; Misassembled During Installation
DURING INSTALLATION OF THE SYSTEM, IT WAS FOUND THAT A COUPLE OF THE RAIL CONNECTION BLOCKS WERE MIS-ALIGNED IN THE CEILING UNISTRUT. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16591773 ↗MalfunctionFeb 7, 2023Flare or Flash; Flare or Flash
WHILE THE SYSTEM WAS BEING USED FOR A FLUOROSCOPY STUDY, THE MAINS CABINET STARTED MAKING LOUD POPPING SOUNDS ALONG WITH SPARKING, SMOKING, AND AN ELECTRICAL FIRE INSIDE OF THE CABINET. NOBODY WAS INJURED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16313564 ↗MalfunctionDec 17, 2020Radiation Output Problem; Radiation Output Problem
DURING ANNUAL PHYSICS TESTING, THE STABILIZED DOSE IS HIGH DURING CONTINUOUS FLUOROSCOPY AND PULSED FLUOROSCOPY FOR 20 AND 30 FRAMES PER SECOND.
Patient problems: No Patient Involvement
MAUDE report 11027848 ↗
Other Philips Medical Systems DMC GmbH products
All Philips Medical Systems DMC GmbH devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page