CombiDiagnost R90Recalls & 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 CombiDiagnost R90 model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 20
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 5
We found 2 models of CombiDiagnost R90 by Philips Medical Systems DMC GmbH in the FDA's device registry (GUDID). Together they are named in 20 adverse event reports in the FDA's MAUDE database, received between Aug 12, 2019 and Sep 29, 2026 — classified as 1 injury, 19 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (7 reports).
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
CombiDiagnost R90 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-0462-2026 · Root cause: Device Design · Recall details · FDA record ↗
- Sep 21, 2023Open, Classified
Potential for units suspended on the ceiling to fail and fall.
Z-0271-2024 · Root cause: Under Investigation by firm · names 2 of these models · Recall details · FDA record ↗
- Feb 11, 2022Open, Classified
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.
Z-1088-2024 · Root cause: Software design · Recall details · FDA record ↗
- Feb 11, 2022Open, Classified
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.
Z-1087-2024 · Root cause: Software design · 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-1355-2023 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗
Most reported CombiDiagnost R90 problems
Device problems
- Detachment of Device or Device Component7
- Device Fell5
- Device Handling Problem4
- Patient Data Problem2
- Device Emits Odor1
- Display or Visual Feedback Problem1
- Insufficient Device Problem Information1
- Manufacturing, Packaging or Shipping Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions17
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
- Unspecified Musculoskeletal problem1
CombiDiagnost R90 models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CombiDiagnost R90 709031System, x-ray, fluoroscopic, image-intensified4 recalls11 reports
- CombiDiagnost R90 709030System, x-ray, fluoroscopic, image-intensified3 recalls9 reports
Recent CombiDiagnost R90 adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Detachment of Device or Device Component
It was reported that the detachable foot table board was broken and would not attach to the table due to physical damage. 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 50934069 ↗InjuryDec 15, 2025Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT THE CEILING SUSPENSION (CS) WAS DIFFICULT TO MOVE, AND AS A RESULT, THE USER EXPERIENCED A BACK INJURY. THE DEVICE WAS IN CLINICAL USE.
Patient problems: Unspecified Musculoskeletal problem
MAUDE report 23800305 ↗MalfunctionOct 17, 2025Detachment of Device or Device Component; Insufficient Device Problem Information; Detachment of Device or Device Component; Insufficient Device Problem Information
IT WAS REPORTED THAT THE CRACK IN THE MOUNTING POSITION OF THE ACTUATOR. THE USE OF DEVICE WAS UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23321489 ↗MalfunctionAug 26, 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 NOT IN CLINICAL USE AND THERE WAS NO HARM TO PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22892437 ↗MalfunctionMay 22, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE BASE WHERE THE PATIENT WAS PLACED HAD BROKEN. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM. ADDITIONAL INFORMATION RECEIVED THAT THE WHEEL INSIDE THE FOOTREST WAS BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22069033 ↗MalfunctionApr 23, 2025Unintended System Motion; Unintended System Motion
IT WAS REPORTED THAT ON COMBIDIAGNOST R90 INDICATING THAT TABLE UP DOWN MOVEMENT IS NOT STRAIGHT INTERMITTENTLY AND MIGHT CAUSE HARM TO THE PATIENT. THERE WAS NO ACTUAL HARM REPORTED TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21891546 ↗MalfunctionMar 31, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THE FOOTSTEP WHERE THE PATIENT CAN STAND ON IT HAS COME OFF / SEEMS TO BE BROKEN. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21733383 ↗MalfunctionNov 28, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE DURING PREPARATION OF EXAMINATION, WHEN THE TABLE WAS BEING TITLED DOWNWARDS THE FOOT STAND FELL AND BROKE. THERE WAS NO USER IMPACT AND THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20804335 ↗MalfunctionNov 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE DEVICE WAS IN CLINICAL USE WHEN THE FOOTSTEP OF THE TABLE WHERE THE PATIENT STANDS HAS COME AND SEEMS TO BE BROKEN. THERE WAS NO PATIENT OR USER IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20607808 ↗MalfunctionOct 12, 2024Detachment of Device or Device Component; Device Fell; Detachment of Device or Device Component; Device Fell
IT WAS REPORTED THAT DURING CLINICAL USE, WHEN SETTING UP THE ROOM FOR EXAMINATION FOR A THORAX EXAMINATION WHERE THE TABLE WAS VERTICAL WITH SOURCE IMAGE DISTANCE OF 150 CM, THE STAND GEOMETRY OF THE SYSTEM FELL DOWN ON THE FLOOR. THE CHAIN IN THE STAND GEOMETRY SNAPPED WHEN THE USER WAS ATTEMPTING TO TILT UPWARDS AT 5 DEGREE ANGLE RESULTING IN FALLING DOWN OF THE COLLIMATOR AND THE TUBE. IT WAS CONFIRMED THAT THERE WAS NO IMPACT OR INJURY TO THE PATIENT AND THE USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20435005 ↗MalfunctionApr 26, 2024Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
THE CUSTOMER REPORTED THAT THE PORTABLE DETECTOR FAILED THE GAIN CALIBRATION DURING THE QUARTERLY CHECK. A DROPPED DETECTOR CAN LEAD IN WORST CASE TO A FRACTURE IN THE FOOT. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19191028 ↗MalfunctionAug 23, 2023Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
THE CUSTOMER REPORTED THAT THE PORTABLE DETECTOR HAS FALLEN DOWN. A DROPPED DETECTOR CAN LEAD IN WORST CASE TO A FRACTURE IN THE FOOT. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17603346 ↗MalfunctionAug 9, 2023Moisture Damage; Moisture Damage
THE CUSTOMER REPORTED THAT WATER WENT INTO CABLES OF SYSTEM AFTER A WATER PIPE FROM THE BATHROOM BURST. THE CUSTOMER REQUESTED A CHECK OF THE SYSTEM. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17487194 ↗MalfunctionAug 8, 2023Poor Quality Image; Device Handling Problem; Device Fell; Poor Quality Image; Device Handling Problem; Device Fell
THE CUSTOMER REPORTED THAT THE PORTABLE DETECTOR FELL AND HAS NOW ARTEFACTS IN THE IMAGE. A DROPPED DETECTOR CAN LEAD IN WORST CASE TO A FRACTURE IN THE FOOT. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17480266 ↗MalfunctionMar 15, 2023Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS IDENTIFIED THAT AN OBSOLETE SPDU (SYSTEM POWER DISTRIBUTION UNIT) SPARE PART IS INSTALLED IN A COMBIDIAGNOST SYSTEM. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16544522 ↗
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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