Philips recalls Ingenia 1.5T MRI systems with faulty pressure relief valve that may release helium gas causing injury. Affected models include 781341 with specific serial numbers.
Pressure relief valve 42 psi installed in the magnet assembly instead of a 3.75 psi valve, may result in release of helium gas and cause injury
Philips is recalling certain Ingenia 1.5T MRI systems because they have a pressure relief valve set to 42 psi instead of the required 3.75 psi. This could cause helium gas to be released, potentially leading to injury. If you own one of these models, you should contact Philips for details.
The system's pressure relief valve is installed at 42 psi instead of the required 3.75 psi. This higher pressure could cause helium gas to be released unexpectedly, potentially leading to injury.
Medical facilities using the Ingenia 1.5T MRI systems with model number 781341 and specific serial numbers are most at risk. Patients undergoing scans with these systems could be affected.
Check if your MRI system has model number 781341 and serial numbers starting with 84344 or 87019, 87231, or other listed numbers in the recall notice.
Reach out to Philips directly to confirm if your MRI system is affected and get instructions for next steps.
The pressure relief valve is installed at 42 psi instead of the required 3.75 psi, which could cause helium gas to be released unexpectedly and lead to injury.
Model number 781341 with specific serial numbers starting with 84344, 87019, 87231, or other listed numbers in the recall notice.
No, but you should contact Philips to confirm if your system is affected and follow their instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2342-2021 — Philips Philips Hello, I own a Philips that is covered by recall Z-2342-2021 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.
