Philips recalls Evolution Upgrade 1.5T MRI machines with model numbers 782116 and 782148 due to potential alignment errors in MobiView app image reviews. Affected units may show incorrect cross-reference lines when viewing images.
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Philips is recalling certain Evolution Upgrade 1.5T MRI machines that could show alignment errors when using the MobiView app to review images. This might cause inaccurate measurements or misinterpretations of medical scans. Users should check if their device has the listed model numbers.
The MobiView app may display cross-reference lines incorrectly when reviewing MRI images. This could lead to inaccurate measurements or misinterpretations of medical scans, potentially affecting diagnosis or treatment decisions.
MRI machine users who own or operate the Evolution Upgrade 1.5T models with model numbers 782116 or 782148. Patients and medical staff using the MobiView app for image reviews are most at risk of inaccurate measurements.
Check for model numbers 782116 or 782148 on your Philips Evolution Upgrade 1.5T MRI machine. Serial numbers listed in the recall include specific combinations like 41042, 41047, 41080, and others.
Identify if your MRI machine has model numbers 782116 or 782148.
Philips has identified potential alignment errors in the cross-reference line functionality when reviewing images generated with the MobiView application.
Check if your machine has model numbers 782116 or 782148. If so, contact Philips for further instructions.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1793-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1793-2025 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.
