Philips recalls SmartPath to dStream 1.5T devices with model numbers 781260, 782112, 782146 due to potential alignment errors in cross reference line functionality when reviewing images via MobiView app.
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Philips is recalling SmartPath to dStream 1.5T devices with specific model numbers because they may have alignment errors when reviewing images using the MobiView app. This could lead to inaccurate image references, but the recall does not involve immediate safety risks.
The device may show alignment errors in the cross reference line when reviewing images generated through the MobiView application. This could cause inaccurate image references during medical imaging procedures, but it does not pose a direct safety hazard.
Users of Philips SmartPath to dStream 1.5T devices with model numbers 781260, 782112, or 782146 are affected. Patients and healthcare professionals using the device for medical imaging are most at risk due to potential misalignment in image references.
Check for model numbers 781260, 782112, or 782146 on the device. The product was sold through Philips North America and may have specific serial numbers listed in the recall notice.
Identify the model number on your SmartPath to dStream 1.5T device to confirm if it is affected.
Philips recalls these devices due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
The recall does not include a remedy, so users should check the model number to confirm if their device is affected and contact Philips for further guidance.
The recall does not indicate any safety risks; the issue is limited to potential alignment errors in image references during medical imaging.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1788-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1788-2025 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.
