Print version of this report
TGA Action ID RC-2026-RN-00741-1
Type of Product Medical Device
Product Name/Description Philips MR Systems on R11, R12.1.1, and R12.2.0

Multiple models and model numbers
ARTG Number 230064, 372370, 485786
Unique Device Identifier (UDI) N/A
Action Type Product Correction
Action Level Hospital
Hazard Classification Class III
Reason for the Action Philips has identified software problems affecting MR systems on software versions R11, R12.1.1 and R12.2.0. The problems have no associated safety impact and do not prevent the system from functioning in accordance with the intended use; however, they can cause inconvenience for operators.
Instructions for Customers/Users Philips will contact users to schedule a time for a Field Service Engineer to install software R12.2.2 SP1. The expected correction release is January 2027.
Action Commencement Date 6/10/2026
Responsible Entity Philips Electronics Australia Ltd
Contact Information 1800 251 400 - Philips Service Delivery Team