Philips recalls its Achieva 1.5T Initial system with MR Elastography (MRE) due to potential stiffness value errors from specific image reconstruction settings. Affected units have model number 781178.
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.
Philips is recalling its Achieva 1.5T Initial system with MR Elastography (MRE) because certain image reconstruction settings can cause stiffness value errors, potentially leading to inaccurate medical scans. This affects medical imaging equipment used in hospitals and clinics.
The system's image reconstruction settings, when combined with Resoundant's algorithm, can cause the reconstructed voxel size to be too small. This leads to stiffness value errors in the default MRE scan protocol, which may result in inaccurate medical imaging.
Medical facilities using the Philips Achieva 1.5T Initial system with MRE. Patients receiving scans on these systems may be at risk of inaccurate results.
Check for model number 781178 on the Philips Achieva 1.5T Initial system with MR Elastography (MRE). This system was sold starting in 2008 with serial numbers up to 20088.
Verify the model number on your Philips Achieva 1.5T Initial system with MR Elastography (MRE) to confirm it is 781178.
Philips recalls this system because specific image reconstruction settings combined with Resoundant's algorithm can cause stiffness value errors in the default MRE scan protocol.
Check the model number on your system; if it is 781178, you may need to contact Philips for further instructions.
The recall addresses potential inaccuracies in medical imaging, not direct safety risks to users. No injuries have been reported.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1952-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1952-2026 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
