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FDA (Device enforcement)Recalled 2026-04-14class ii

Philips North America: Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178.

Hazard

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

Details from the source

Reason for recall: The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small. Distribution: Worldwide - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Chile, Cuba, Cyprus, Denmark, Ecuador, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Iraq, Israel, Italy, Japan, Kenya, Lebanon, Lithuania, Malta, Mexico, Myanmar, Netherlands, Pakistan, Palestine, Peru, Poland, Portugal, Russian Fed., Singapore, South Korea, Spain, Sweden Quantity: 1 unit Lot/code info: 1. Model Number (REF): 781178. UDI: None. Serial Numbers: 20088.

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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