Philips recalls specific Multiva MRI systems due to potential helium gas release during magnet quench, which could cause injury. Affected models include 1.5T 8 R5, 16 R5, and 8ch R5 systems with model numbers 781072-781078.
Potential risk for helium gas inside the MR examination room during a magnet quench
Philips is recalling certain Multiva MRI systems that may release helium gas during a magnet quench event. This could lead to injury if the helium gas escapes into the examination room. The recall affects specific models sold in the U.S. with model numbers 781072 through 781078.
During a magnet quench, the superconducting magnet in the MRI system can rapidly lose its magnetic field. This process may release helium gas into the examination room. If the helium gas escapes, it could create a risk of injury to people present in the room.
Medical facilities using the recalled Multiva MRI systems are most at risk. Patients undergoing scans with these systems could potentially be exposed to helium gas if a quench occurs.
Check for the model numbers 781072, 781073, 781074, 781076, or 781078 on the Multiva MRI systems. These models were sold in the U.S. as part of the recall.
Reach out to Philips Electronics North America Corporation for assistance with the recall.
The recall affects Multiva 1.5T 8 R5 Model 781072, Multiva 1.5T 16 R5 Model 781073, Multiva 1.5T 8ch R5 Model 781074, Multiva 1.5T Model 781076, and Multiva 1.5T 16ch R5 Model 781078.
The recall states there is a potential risk for helium gas release during a magnet quench, which could cause injury if the gas escapes into the examination room.
Contact Philips Electronics North America Corporation for assistance with the recall.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1430-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-1430-2018 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.
