Philips recalls specific MRI systems due to potential helium gas release during magnet quench, which could cause injury. Affected models include Multiva 16, Multiva 8, and Achieva 1.5T systems. Contact Philips for details.
Potential risk for helium gas inside the MR examination room during a magnet quench
Philips is recalling certain MRI systems that could release helium gas during a magnet quench, potentially causing injury. This risk applies to specific models sold in the U.S. between 2019 and 2021.
The magnet quench process can release helium gas into the examination room. This gas buildup could cause injury if it leads to a sudden pressure change or asphyxiation.
Patients and staff using the recalled MRI systems are at risk. The most vulnerable are those who may be exposed to the helium gas during a magnet quench event.
Check for the model numbers: 781487 (Multiva 16), 781488 (Multiva 8), 781492 (Achieva 1.5T), 781495 (HFO), 781496 (Multiva 16), 781497 (Multiva 8), or 781498 (Ingenia 1.5T CX). These models were sold between 2019 and 2021.
Identify the model number on your MRI system to confirm if it is affected by this recall.
Reach out to Philips for specific instructions on how to address the recall.
The affected models include Multiva 16 (781487), Multiva 8 (781488), Achieva 1.5T (781492), HFO (781495), Multiva 16 (781496), Multiva 8 (781497), and Ingenia 1.5T CX (781498).
The recall states a potential risk for helium gas release during a magnet quench, which could cause injury. However, the exact risk level is not specified in the notice.
Check the model number on your system. Affected models were sold between 2019 and 2021 and include specific model numbers listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1441-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-1441-2018 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.
