DigitalDiagnost C90 712034Recalls & reported problems

Summary

The FDA's MAUDE database contains 90 adverse event reports that list this exact device (DI 00884838090699), received between Jun 15, 2021 and Sep 24, 2026 — classified as 5 injuries, 85 malfunctions.

The most frequently reported specific device problem is “Device Fell” (72 reports).

3 FDA recall records name this device's identifier, 3 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 16, 2026.

Recalls naming this device

1. 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-0465-2026 · Root cause: Device Design · Recall details · FDA record ↗

2. Sep 21, 2023Open, Classified

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

   Z-0276-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

3. May 19, 2023Open, Classified

   There is a software login in issue that may prevent the user from logging in.

   Z-2042-2023 · Root cause: Software change control · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 90 reports, in the reporter's own words as published by the FDA.

• InjurySep 24, 2026Mechanical Jam

  It was reported that the system did not release efficiently while in use and the customer had to drag the tube head. They also noted that the pulling of the system was also a problem and was severely straining on their shoulders. Additional information has been requested from the customer to clarify the allegations and support further investigation and assessment, and a response is currently pending.

  Patient problems: Insufficient Information

  MAUDE report 50881325 ↗
• InjurySep 24, 2026Mechanical Jam

  It was reported that the Comfort Positioning feature was not performing as intended while the device was in clinical use. It was further alleged that multiple workers' compensation incidents had occurred as a result of the issue. However, the information currently available is insufficient to adequately assess the reported events. Additional information has been requested from the customer to clarify the allegations and support further investigation and assessment, and a response is currently pending.

  Patient problems: Insufficient Information

  MAUDE report 50881324 ↗
• InjurySep 24, 2026Mechanical Jam

  It was reported that the Comfort Positioning feature was not performing as intended while the device was in clinical use. It was further alleged that multiple workers' compensation incidents had occurred as a result of the issue. However, the information currently available is insufficient to adequately assess the reported events. Additional information has been requested from the customer to clarify the allegations and support further investigation and assessment, and a response is currently pending.

  Patient problems: Insufficient Information

  MAUDE report 50880756 ↗
• MalfunctionApr 3, 2026Detachment of Device or Device Component

  IT WAS REPORTED THAT THE DAMPER ON WALL TRIPOD BROKEN OFF. 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 24777074 ↗
• MalfunctionDec 19, 2025Circuit Failure; Smoking; Insufficient Device Problem Information; Circuit Failure; Smoking; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE SYSTEM DOWN DUE TO UB BOARD BURNT. 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 23849379 ↗
• MalfunctionDec 9, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE THERE ARE ARTIFACTS ON THE BIG CASSETTE. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23755207 ↗
• MalfunctionDec 9, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE PORTABLE DETECTOR DROP. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23755100 ↗
• MalfunctionDec 9, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR DROPPED AND CUSTOMER NEEDS NEW 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 23754728 ↗
• MalfunctionDec 2, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR MECHANICALLY DAMAGED. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23692334 ↗
• MalfunctionNov 24, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR FELL FROM A STOOL, AND THE USER ASKED WHETHER IT COULD STILL BE USED NORMALLY. THE DEVICE REMAINED IN CLINICAL USE, AND NO HARM OCCURRED TO EITHER THE PATIENT OR THE USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23633717 ↗
• MalfunctionNov 19, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTORS NOT CALIBRATING. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR DROPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23591572 ↗
• MalfunctionNov 19, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR HAS FALLEN AND IT IS GOING INTO INITIALIZATION MODE.THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23591448 ↗
• MalfunctionNov 13, 2025Device Handling Problem; Device Handling Problem

  IT WAS REPORTED THAT THE CABLE HOLDER SLIPPED FROM THE CS (CEILING SUSPENSION) RAILS AND FELL ON THE TABLE AND NEEDS TABLE REPLACEMENT. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23544192 ↗
• MalfunctionOct 15, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT DURING AN X-RAY OF THE FOOT, THE PATIENT RAISED HIS LEG, CAUSING THE SENSOR TO FALL TO THE GROUND. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23300938 ↗
• MalfunctionAug 13, 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 22790909 ↗
• MalfunctionAug 11, 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. ADDITIONAL INFORMATION RECEIVED AND CONFIRMED THAT THE DETECTOR WAS DROPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22769571 ↗
• MalfunctionAug 8, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR WAS DROPPED AND WANTED TO CHECK LOGS. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22747253 ↗
• MalfunctionJul 30, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE FLAT PANEL SENSOR NO LONGER WORKS (DETECTOR HAS FALLEN). THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22662850 ↗
• MalfunctionJul 28, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE HORSESHOE IS NO LONGER RELEASED. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR WAS DROPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22628622 ↗
• MalfunctionJul 21, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR DROPPED AND NOT WORKING. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22553077 ↗
• MalfunctionJul 10, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE SKYPLATE DETECTOR PRODUCED GRAY IMAGES AND IS NOT READY. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR WAS DROPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22466100 ↗
• MalfunctionJun 9, 2025Fire; Sparking; Fire; Sparking

  IT WAS REPORTED THAT THE UA BOARD WAS BURNT. THE USAGE OF THE DEVICE AT THE TIME OF THE INCIDENT IS UNKNOWN AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22169268 ↗
• MalfunctionJun 2, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR WAS DROPPED. 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 22121835 ↗
• MalfunctionJun 2, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR HAS ARTIFACTS. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR WAS DROPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22121705 ↗
• MalfunctionMay 13, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE DETECTOR DOES NOT PASS CALIBRATION. THE DEVICE WAS NOT IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR HAD BEEN DROPPED AND HAD HARD AND MEDIUM SHOCKS WERE REGISTERED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22010796 ↗