ClearanceBrief
Recall Z-2213-2025 · LNH System, Nuclear Magnetic Resonance Imaging

Philips North America

MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152;

DateJul 30, 2025 (initiated Jun 30, 2025)
StatusOpen, Classified
ReasonThe potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
Root causeDevice Design
ActionOn June 30, 2025, URGENT MEDICAL DEVICE CORRECTION letters were sent to customers. 4. Actions that should be taken by the customer / user in order to prevent risks for patients or users 4.1. When using any affected system identified according to the information in section 3, follow the instructions below. 4.2. Pay particular attention if a scan interruption occurs and a scan abort symbol is encountered, which may appear in the user interface (UI) with the symbols shown in Figure 4 below: Figure 4. Scan Abort Symbols 4.3. When scan aborts occur the symbol is shown and applicable messages are
Quantity551 units
DistributionWorldwide distribution - US Nationwide and the countries of Albania, Algeria, Andorra, Angola, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Belize, Bolivia, Bosnia-Herz., Brazil, Bulgaria, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, C¿te D'Ivoire, Croatia, Cu
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K212673MR 5300
Philips Medical Systems Nederland B.V., Nov 19, 2021
K223442MR 5300 and MR 7700 R11 MR Systems
Philips Medical Systems Nederlands B.V., Dec 23, 2022