Philips recalls Intera 1.0T MRI scanners (Stellar Model 781102, Pular Model 781103) due to potential helium gas release during magnet quench, which could cause safety hazards in MRI rooms.
Potential risk for helium gas inside the MR examination room during a magnet quench
Philips is recalling specific Intera 1.0T MRI scanners that may release helium gas during a magnet quench. This risk could lead to safety hazards in the MRI examination room if the device is used without proper precautions.
The scanners can release helium gas during a magnet quench, which is a process where the superconducting magnet loses its magnetic field. This gas release could create a sudden pressure change in the MRI room, potentially causing safety hazards.
MRI facility staff and patients using the recalled scanners. Those operating the equipment in MRI rooms are most at risk during magnet quench events.
Check for the Stellar Model 781102 or Pular Model 781103 on the scanner. These models were sold by Philips Electronics North America Corporation for MRI diagnostic use.
Identify the model number on your scanner to confirm if it is a recalled Stellar Model 781102 or Pular Model 781103.
The scanners may release helium gas during a magnet quench, which could create a sudden pressure change in the MRI room, potentially causing safety hazards.
Check for the Stellar Model 781102 or Pular Model 781103 on the scanner. These models were sold by Philips Electronics North America Corporation for MRI diagnostic use.
The recall record 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-1432-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-1432-2018 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.
