CombiDiagnost R90 709031Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 00884838101456), received between Sep 29, 2021 and Sep 29, 2026 — classified as 1 injury, 10 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (5 reports).

4 FDA recall records name this device's 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, 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-0462-2026 · Root cause: Device Design · Recall details · FDA record ↗

2. Sep 21, 2023Class IIOpen, Classified

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

   Z-0271-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

3. Feb 11, 2022Class IIOpen, 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 ↗

4. 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-1355-2023 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 11 most recent of 11 reports, 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 ↗
• 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 ↗
• 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 ↗
• MalfunctionDec 28, 2021Patient Data Problem; Patient Data Problem

  THE CUSTOMER REPORTED THAT ONE IMAGE OF A PATIENT WAS DISPLAYED IN AN OTHER PATIENT'S FOLDER. THERE WAS NO HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13099197 ↗
• MalfunctionDec 6, 2021Patient Data Problem; Patient Data Problem

  THE CUSTOMER REPORTED THAT ONE IMAGE OF A PATIENT WAS DISPLAYED IN AN OTHER PATIENT'S FOLDER. THERE WAS NO HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12934779 ↗
• MalfunctionSep 29, 2021Display or Visual Feedback Problem; Display or Visual Feedback Problem

  THE CUSTOMER REPORTED THAT THE CURRENT IMAGE IS MIXED WITH THE PREVIOUS IMAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12547062 ↗