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TGA Action ID RC-2025-RN-00942-1
Type of Product Medical Device
Product Name/Description Philips Diagnostic X-Ray (DXR) systems

DigitalDiagnost 4
Product code: 712031

DigitalDiagnost C90
Product code: 712034

Radiography 7300 C
Product code: 712037

Muliple Model Numbers
ARTG Number 390959
Unique Device Identifier (UDI) N/A
Action Type Product Correction
Action Level Hospital
Hazard Classification Class II
Reason for the Action 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 problems.

As of September 2025, Philips has received 43 complaints associated with this problem. There has been one report where two users experienced minor shoulder injury as a result of this defect.
Instructions for Customers/Users Philips will contact customers to schedule a time for a Field Service Engineer to inspect the ceiling suspension and implement a follow-up hardware correction, if required.

The initial inspection and corrections including minor ceiling suspension adjustment will commence by end of Q4 2025.
Action Commencement Date 5/11/2025
Responsible Entity Philips Electronics Australia Ltd
Contact Information 1800 251 400 - Philips Service Delivery Team