Philips recalls Ingenia 1.5T CX MRI scanners (models 781261 & 781262) due to potential helium gas release in the magnet quench process, which could create hazardous conditions in the exam room.
Potential risk for helium gas inside the MR examination room during a magnet quench
Philips is recalling two specific models of MRI scanners (781261 and 781262) because they might release helium gas during a magnet quench event. This could create hazardous conditions in the MRI room, potentially affecting patient safety during scans.
During a magnet quench (when the MRI's superconducting magnet loses its magnetic field), the system may release helium gas into the examination room. This gas could accumulate and create hazardous conditions, potentially affecting patient safety.
Healthcare facilities using Philips Ingenia 1.5T CX MRI scanners with model numbers 781261 or 781262 are affected. Patients undergoing scans in these machines may be at risk if helium gas is released during a magnet quench.
Check if your MRI scanner has model numbers 781261 or 781262. These models are part of the Philips Ingenia 1.5T CX series used for diagnostic imaging.
Identify the model number on your Philips Ingenia 1.5T CX scanner to confirm if it is 781261 or 781262.
The recall is due to potential helium gas release during a magnet quench event, which could create hazardous conditions in the MRI examination room.
The official recall notice does not specify a remedy or action for affected units.
The recall indicates a potential hazard but does not specify the severity or likelihood of injury.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1437-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-1437-2018 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.
