DigitalDiagnostRecalls & reported problems across all models
Philips Medical Systems DMC GmbH · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name at least one DigitalDiagnost model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 81
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 4
We found 4 models of DigitalDiagnost by Philips Medical Systems DMC GmbH in the FDA's device registry (GUDID). Together they are named in 81 adverse event reports in the FDA's MAUDE database, received between Jul 11, 2019 and Jun 30, 2026 — classified as 81 malfunctions.
The most frequently reported specific device problem is “Device Fell” (68 reports).
4 FDA recall records name at least one of these models by its device identifier, 4 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
DigitalDiagnost 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-0464-2026 · Root cause: Device 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-0274-2024 · Root cause: Under Investigation by firm · 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-0273-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 21, 2023Open, Classified
Potential for units suspended on the ceiling to fail and fall.
Z-0272-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported DigitalDiagnost problems
Device problems
- Device Fell68
- Device Handling Problem67
- Detachment of Device or Device Component7
- Poor Quality Image4
- Fire2
- Electrical /Electronic Property Problem1
- Inappropriate/Inadequate Shock/Stimulation1
- Power Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions80
- Shock1
DigitalDiagnost models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- DigitalDiagnost 712031Solid state x-ray imager (flat panel/digital imager)2 recalls65 reports
- DigitalDiagnost 712032Solid state x-ray imager (flat panel/digital imager)2 recalls10 reports
- DigitalDiagnost 712033Solid state x-ray imager (flat panel/digital imager)1 recall6 reports
- DigitalDiagnost 712226Solid state x-ray imager (flat panel/digital imager)1 recall0 reports
Recent DigitalDiagnost adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJun 30, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT THE PATIENT STEP PLATE ON THE ENTIRE TRIPOD HAD BROKEN OFF AT THE BACK. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO HARM TO THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25663720 ↗MalfunctionJun 5, 2026Fire
IT WAS REPORTED THAT A FIRE INCIDENT HAD OCCURRED WITHIN THE HOSPITAL FACILITY OVER THE WEEKEND. AS A RESULT OF THE INCIDENT, SMOKE ENTERED THE ROOM WHERE THE PHILIPS SYSTEM WAS INSTALLED THROUGH CABLE DUCTS CONNECTED TO ADJACENT AREAS. AS A PRECAUTIONARY MEASURE, THE CUSTOMER DISCONNECTED THE ACQUISITION WORKSTATION (AWS) AND REQUESTED VERIFICATION OF SYSTEM FUNCTIONALITY BEFORE RETURNING THE EQUIPMENT TO SERVICE. THE DEVICE WAS OUTSIDE OF CLINICAL USE AT THE TIME OF THE EVENT, AND NO PATIENT OR USER HARM WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25410919 ↗MalfunctionApr 1, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT THE STITCHING STAND HYDRAULIC RAM HAS COME LOOSE. THE DEVICE WAS NOT IN CLINICAL USE, AND THERE WAS NO HARM TO THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24751380 ↗MalfunctionMar 2, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT THE PATIENT SUPPORT PROBLEM. THE DEVICE WAS NOT IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24481127 ↗MalfunctionDec 16, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE REMOTE ALERT OF A MECHANICAL HEAVY SHOCK TO THE DETECTOR. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO HARM TO PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23818701 ↗MalfunctionDec 16, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE SKYPLATE DETECTOR DROPPED AND HEAVY SHOCK REGISTERED TO THE DETECTOR. THE DEVICE WAS NOT IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23818699 ↗MalfunctionDec 16, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE REMOTE ALERT OF A HEAVY SHOCK TO THE DETECTOR. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO HARM TO PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23818691 ↗MalfunctionDec 15, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE DETECTOR WAS DROPPED AND NOW IT WILL NOT CALIBRATE. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23800128 ↗MalfunctionDec 10, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE SKYPLATE DETECTOR WAS NOT PASSING CALIBRATION AND WAS GETTING A MESSAGE THAT THE DOSE WAS TOO LOW. THE DEVICE WAS NOT IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23766643 ↗MalfunctionDec 9, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE LARGE MOBILE DETECTOR FAILED, AND UNDERTABLE MOUNTING WAS NOT POSSIBLE. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23756851 ↗MalfunctionNov 27, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE SKYPLATE NOT WORKING. THE DEVICE WAS NOT IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23665133 ↗MalfunctionNov 26, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE ON-SWITCH OF THE DIGITAL DETECTOR CAN NO LONGER BE OPERATED PROPERLY. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23655170 ↗MalfunctionNov 25, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE SKYPLATE WAS DROPPED AND NOW FACING ISSUES. THE DEVICE WAS NOT IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23646201 ↗MalfunctionNov 21, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE REMOTE ALERT OF A MECHANICAL HEAVY SHOCK TO THE DETECTOR. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO HARM TO PATIENT OR USER. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR HAD BEEN DROPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23615275 ↗MalfunctionNov 18, 2025Power Problem; Power Problem
IT WAS REPORTED THAT GENERATOR ERROR OBSERVED AFTER A POWER OUTAGE. THE USE OF DEVICE WAS UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23583422 ↗
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.
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