Radiography 7300 C 712037Recalls & reported problems
Philips Medical Systems DMC GmbH · Radiography 7300 C is a high-end digital radiography system consisting of a height adjustable patient support table and a ceiling suspension consisting of a tube including a control handle used to acquire images with a flat panel fixed RAD detector. Additionally, different vertical stands for the radiography examinations are available. The ceiling suspension can be moved in longitudinal and lateral directions and additionally the tube can be tilted and rotated as well. The proposed Radiography 7300 C is configured with a Philips x-ray generator and a flat panel fixed RAD detector, Pixium 4343RCE. Together with the tube these components form the radiography Image Chain. The additional option of the portable wireless detector i.e. the SkyPlate family can be used for free exposures as well as in the patient support table or in the vertical stand. The proposed Radiography 7300 C uses the following Accessories, • Parking frame for accessories • Handgrips • Side Bar • Adjustable straps • Compression Belt • Infusion Bottle holder TH-S • Infusion Bottle holder TH2 • Support for CPR (Cardio Pulmonary Resuscitation) • Stretch Grip • Remote control holder • Charger 2EZ • Grid’s for Skyplayte Wireless Portable Detectors • Grid’s for Fixed Detectors • Detector Handle • Detector holder for patient bed • Mobile detector holder • Portable panel protector • WPD Hygienic bags • Patient support • Adjustable Straps for Patient Support • Stitching Ruler Radiography 7300C is a successor of DigitalDiagnost C90 (Release Version 1.1). The main differences of Radiography 7300 C versus DigitalDiagnost C90 are optional new features: • Assisted collimation & Assisted detector height alignment (Smart Collimation Thorax / SCT) • Overlays including On-screen collimation & AEC Visualization · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 8
- Deaths reported
- 1
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00884838116016), received between Mar 11, 2025 and Sep 16, 2026 — classified as 1 death, 1 injury, 6 malfunctions.
The most frequently reported specific device problem is “Device Fell” (4 reports).
1 FDA recall record name this device's identifier, 1 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.
Reports received per month
Recalls naming this device
- 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-0466-2026 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Device Fell4
- Device Handling Problem4
- Mechanical Jam3
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Pain2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Fall1
- Muscle/Tendon Damage1
- Neck Stiffness1
- Unspecified Musculoskeletal problem1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Mechanical Jam
Patient problems: Neck Stiffness
MAUDE report 50787850 ↗MalfunctionAug 27, 2026Mechanical Jam
It was reported that the Ceiling Suspension (CS) was difficult to move in all directions, including longitudinal and transverse movement. The device was in clinical use and one radiographer reported experiencing a strained shoulder associated with use of the room.
Patient problems: Muscle/Tendon Damage; Pain
MAUDE report 50472977 ↗InjuryDec 15, 2025Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT THE SYSTEM WAS NOT TRACKING PROPERLY AND THE TUBE WAS VERY DIFFICULT TO MOVE MANUALLY. THIS RESULTED IN A SHOULDER INJURY TO THE USER, AND OTHER STAFF MEMBERS WERE UNABLE TO USE THE ROOM. THE DEVICE WAS NOT IN CLINICAL USE AT THE TIME, AND NO PATIENT HARM OCCURRED.
Patient problems: Pain; Unspecified Musculoskeletal problem
MAUDE report 23802519 ↗MalfunctionNov 20, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE DETECTOR WAS DROPPED AND CUSTOMER WANTS TO KNOW IF IT'S SAFE TO USE. 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 23601595 ↗MalfunctionOct 29, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE IMMEDIATE SHOT DETECTED AT 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 23412459 ↗MalfunctionOct 15, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THIRD DETECTOR DOES NOT BIND. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23276991 ↗DeathMar 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT DURING A PATIENT EXAMINATION, AN OLD AGE PATIENT FELL OFF FROM THE TABLE WHILE THE OPERATOR WAS IN THE CONTROL ROOM. SIX DAYS LATER, THE PATIENT PASSED AWAY IN THE HOSPITAL, THOUGH IT'S UNCLEAR WHETHER THE FALL CONTRIBUTED TO THE DEATH. THE FALL OCCURRED ONLY ONCE AND WAS PROMPTLY FOLLOWED UP WITH A CT SCAN FOR INJURIES. THERE WAS NO IMPACT TO THE USER. THE PATIENT IMPACT IS DEATH.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Fall
MAUDE report 21660800 ↗MalfunctionMar 11, 2025Device Handling Problem; Device Fell; Device Handling Problem; Device Fell
IT WAS REPORTED THAT THE SKYPLATE FELL AND HAS ARTIFACTS IN IMAGE. THE DEVICE WAS IN CLINICAL USE AND THERE WAS NO HARM TO PATIENT OR USER. ADDITIONAL INFORMATION RECEIVED THAT THE DETECTOR WAS DROPPED BY THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21570761 ↗
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- Proteus XRaGE Hualun Medical Systems Co., Ltd · System, x-ray, stationary2 recalls0 reports
- FDR Visionary Suite 566-16130-33Shimadzu Corporation · System, X-Ray, Stationary2 recalls0 reports
- DigitalDiagnost C50Philips Healthcare (Suzhou) Co., Ltd. · System, x-ray, stationary1 recall8 reports
- DigitalDiagnost C50Philips Healthcare (Suzhou) Co., Ltd. · System, x-ray, stationary1 recall5 reports
- DRX-Compass X-ray SystemCarestream Health, Inc. · System, x-ray, stationary1 recall2 reports
- SEDECAL SEDECAL X URSSedecal · System, X-Ray, Stationary1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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