Philips recalls two model numbers of 1.5T MRI scanners with MR Elastography (MRE) due to potential stiffness value errors from image reconstruction settings.
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 two specific model numbers of their 1.5T MRI scanners that use MR Elastography (MRE) technology. The issue could cause the scanner to display incorrect stiffness values in medical images, which might affect diagnosis accuracy.
The scanner's image reconstruction settings, when combined with a specific algorithm, can cause the displayed voxel size to be too small. This may lead to incorrect stiffness measurements in medical images, potentially affecting diagnosis accuracy.
Medical facilities using Philips Achieva 1.5T MRI scanners with model numbers 781196 or 781296 are affected. Patients undergoing scans on these models may be at risk of inaccurate medical imaging results.
Check for model numbers 781196 or 781296 on the scanner. Serial numbers for model 781196 are 21957, and for model 781296 are 32039 or 32095.
Identify the model number on your Philips Achieva 1.5T MRI scanner to see if it is 781196 or 781296.
Philips recalls these models because image reconstruction settings can cause stiffness value errors in MR Elastography scans, potentially affecting diagnosis accuracy.
Check for model numbers 781196 or 781296. Model 781196 has serial number 21957, and model 781296 has serial numbers 32039 or 32095.
The recall does not specify a remedy, so contact Philips directly for guidance on next steps.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1951-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1951-2026 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.
