Philips recalls 1.5T MRI conversion devices (Model 781260) due to potential helium gas release during magnet quench, which could create unsafe conditions in MRI rooms.
Potential risk for helium gas inside the MR examination room during a magnet quench
Philips is recalling its Conversion SmarthPath to dStream 1.5T MRI machines (Model 781260) because they might release helium gas during a magnet quench. This could create unsafe conditions in MRI examination rooms if the gas accumulates.
During a magnet quench (when the MRI's superconducting magnet loses its magnetic field), the device might release helium gas. If this gas accumulates in the MRI room, it could create unsafe conditions for patients and staff.
Medical facilities using Philips Conversion SmarthPath to dStream 1.5T MRI machines (Model 781260) are affected. Patients and staff in MRI rooms are at risk if helium gas accumulates during a magnet quench.
Check for the model number 781260 on Philips Conversion SmarthPath to dStream 1.5T MRI machines. These devices were sold starting from 2007.
Look for the model number 781260 on the device.
Contact Philips customer service for specific instructions on handling the device.
The model number is 781260.
The device might release helium gas during a magnet quench, which could create unsafe conditions in MRI rooms.
The recall record does not mention a fix or remedy.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1436-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-1436-2018 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.
