ClearanceBrief
Recall Z-1798-2025 · LNH System, Nuclear Magnetic Resonance Imaging

Philips North America Llc

Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;

DateMay 16, 2025 (initiated May 13, 2025)
StatusOpen, Classified
ReasonPotential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Root causeSoftware design
ActionOn May 12, 2025 URGENT MEDICAL DEVICE CORRECTION letters were sent to customers. Actions that should be taken by the customer / user in order to prevent risks for patients or users You may continue to use your system(s) in accordance with the intended use. A. To avoid the potential issue of an incorrect cross reference line in MobiView generated images, use the same voxel size and field of view across all station scans. B. Do not use cross reference line functionality in box mode, all slices mode, or 3D mode. Use the cross reference line functionality in single slice mode. Circulate this not
Quantity152 units (25 US, 127 OUS)
DistributionWorldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ire
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K193215Achieva, Intera, Ingenia, Ingneia CX, Ingenia Elition, and Ingenia Ambition MR Systems
Philips Medical Systems Nederland B.V., Apr 10, 2020
K213583Achieva, Ingenia, Ingenia CX, Ingenia Elition and Ingenia Ambition MR Systems
Philips Medical Systems Nederland B.V., May 16, 2022