Philips recalls T5 Model 78104 MRI scanners due to potential helium gas release during magnet quench, which could create unsafe conditions in medical facilities.
Potential risk for helium gas inside the MR examination room during a magnet quench
Philips is recalling its T5 Model 78104 MRI scanners because they may release helium gas during a magnet quench event. This poses a risk to medical staff and patients in the examination room. The recall is specific to MRI machines used for diagnostic imaging.
During a magnet quench, the MRI's superconducting magnet can rapidly lose its magnetic field. This process may release helium gas into the examination room, creating a risk of asphyxiation or other hazards for people present.
Medical facilities using Philips T5 Model 78104 MRI scanners are most at risk. Patients and staff in the examination room during a magnet quench could be affected.
The recalled product is Philips T5 Model 78104 MRI scanners used for diagnostic imaging. These were sold starting from the product's initial release date.
Identify if your MRI scanner is the Philips T5 Model 78104 by checking the product label or documentation.
The recall is due to potential helium gas release during a magnet quench event, which could create unsafe conditions in the examination room.
The official recall notice does not specify a remedy or action steps for affected users.
The recall indicates a potential risk during magnet quench events, but the exact impact on patients is not detailed in the official notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1442-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-1442-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
