DigitalDiagnost C90 712035Recalls & reported problems

Summary

The FDA's MAUDE database contains 17 adverse event reports that list this exact device (DI 00884838090705), received between Sep 19, 2023 and Sep 16, 2026 — classified as 17 malfunctions.

The most frequently reported specific device problem is “Device Fell” (16 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 16, 2026.

Recalls naming this device

1. May 1, 2026Open, Classified

   System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

   Z-2354-2026 · Root cause: Device Design · Recall details · FDA record ↗

2. 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 ↗

3. Sep 21, 2023Open, Classified

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

   Z-0275-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

4. 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 17 most recent of 17 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 16, 2026Mechanical Jam

  It was reported that the Comfort Positioning feature was not performing as intended while the device was in clinical use. A Good Faith Effort (GFE) was initiated which confirmed that only one user was affected by the reported issue. The user, sustained a minor strain to their right (dominant) shoulder and was assessed by their general practitioner, including an ultrasound scan. No further treatment or medical intervention was required. The user has fully recovered, with no expected impact on function or range of motion.

  Patient problems: Muscle/Tendon Damage

  MAUDE report 50785869 ↗
• MalfunctionFeb 2, 2026Insufficient Device Problem Information; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE TUBE CASING HAS COME LOOSE. 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 24232718 ↗
• MalfunctionNov 19, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE REMOTE ALERT TRIGGERED FROM THE DETECTOR. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23591939 ↗
• MalfunctionNov 7, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT AN ARTIFACT ON THE SKYPLATE DETECTOR COULD NOT BE CLEARED. THE DEVICE WAS IN CLINICAL USE AT THE TIME OF THE EVENT, AND NO HARM OCCURRED TO THE PATIENT OR USER. ADDITIONAL INFORMATION LATER CONFIRMED THAT THE DETECTOR HAD BEEN DROPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23495067 ↗
• MalfunctionSep 15, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE SKYPLATE NO LONGER 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 23048594 ↗
• MalfunctionJul 16, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22517000 ↗
• MalfunctionJul 4, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22401821 ↗
• MalfunctionMay 26, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THAT THE SKYPLATE WAS DROPPED AND IS NOW CAUSING ARTIFACT. NEEDS TO BE REPLACED. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22083569 ↗
• MalfunctionMar 3, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THE DETECTOR WAS DROPPED. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR HAS RECORDED MEDIUM SHOCKS, HOWEVER THERE WERE NO PHYSICAL DAMAGE TO THE DETECTOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21505248 ↗
• MalfunctionDec 30, 2024Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  IT WAS REPORTED THE DETECTOR DOES NOT STAYS IN PLACE ON WALL STAND BUCKY AND THAT IT MIGHT HAVE DROPPED. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21033137 ↗
• MalfunctionJun 17, 2024Use of Device Problem; Device Fell; Use of Device Problem; Device Fell

  IT WAS REPORTED THAT THE IMAGES HAD BANDS POSSIBLY DUE TO SENSOR ISSUES. 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 19554386 ↗
• MalfunctionMay 15, 2024Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  THE ISSUE REPORTED WAS THAT THE PORTABLE DETECTOR STOPPED COMMUNICATING WITH THE EQUIPMENT AFTER A FALL . THERE'S NO ALLEGATION OF DEATH OR SERIOUS INJURY. BASED ON THE AVAILABLE INFORMATION, THIS ISSUE HAS BEEN DETERMINED NOT TO BE A REPORTABLE EVENT. PHILIPS HAS STARTED THE INVESTIGATION OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19317490 ↗
• MalfunctionMay 2, 2024Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  THE CUSTOMER REPORTED THAT THE PORTABLE DETECTOR DROPPED. 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 19228147 ↗
• MalfunctionMar 27, 2024Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  THE CUSTOMER REPORTED THAT THE PORTABLE DETEKTOR DROPPED. 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 18987400 ↗
• MalfunctionMar 20, 2024Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  THE CUSTOMER REPORTED THAT THE PORTABLE DETECTOR FELL DOWN DURING POSITIONING UNDER A PATIENT. 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 18939354 ↗
• MalfunctionJan 18, 2024Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  THE CUSTOMER REPORTED THAT THE PORTABLE DETECTOR DROPPED AND NEEDS TO BE CHECKED. 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 18533049 ↗
• MalfunctionSep 19, 2023Device Handling Problem; Device Fell; Device Handling Problem; Device Fell

  THE CUSTOMER REPORTED THAT A PORTABLE DETECTOR FELL AND IT REGISTERED A SHOCK. 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 17772702 ↗