ClearanceBrief
Recall Z-3242-2026 · LNH System, Nuclear Magnetic Resonance Imaging

Philips North America Llc

MR 7700 and Upgrade to MR 7700; Model Number (REF): 1. 782120, 2. 782153, 3. 782130 (Upgrade);

DateSep 18, 2026 (initiated Aug 21, 2026)
StatusOpen, Classified
ReasonA software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.
Root causeSoftware design
ActionOn August 24, 2026 URGENT Medical Device Correction letters were sent to customers. Actions to be taken: " To prevent this issue from occurring, o Use the standard 3D Vane scan protocol from the Philips Examcard Database, or o For custom 3D Vane scan protocols, use a maximum of 480 for the reconstruction matrix and use a maximum of 167 for the number of slices. " You may continue to use affected systems in accordance with their intended use. " Circulate this notice to all users or new owners of this device so that they are aware of the issues and associated hazard/harm. " Please retain this Ur
Quantity37
DistributionWorldwide distribution - US Nationwide and the countries of Albania, Algeria, Andorra, Angola, Argentina, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Belize, Bolivia, Bosnia and Herzegovina, Brazil, Bulgaria, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, C¿te D'
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K213516Ingenia 3.0T, Ingenia 3.0T CX, Ingenia Elition and MR 7700 with Distributed Multi Nudclei
Philips Medical Systems Nederland B.V., Mar 3, 2022
K230972Ingenia Elition and MR 7700 MR Systems
Philips Medical Systems Nederland B.V., Apr 28, 2023