Philips recalls Ingenia 1.5T S MRI systems with model number 781347 due to potential gradient coil failures that could cause smoke or fire. Affected units include specific serial numbers listed in the recall notice.
The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.
Philips is recalling certain Ingenia 1.5T S MRI systems because a component in the gradient coil might overheat and cause smoke or fire. This could lead to serious injury or property damage if the system is used without correction.
The gradient coil in the affected MRI systems may fail and act as a heat source, potentially producing smoke or fire. This could happen during normal operation, especially if the system is used without proper maintenance or if the component overheats.
Medical facilities using the specific Ingenia 1.5T S MRI systems with model number 781347 and serial numbers listed in the recall are most at risk. Patients and staff could be affected if the system malfunctions.
Check if your MRI system has model number 781347 and serial numbers listed in the recall notice (e.g., 81001, 81003, etc.). The recall applies to specific units sold in the U.S. by Philips North America.
Verify your MRI system's model number and serial numbers against the list provided in the recall notice to confirm if it is affected.
Reach out to Philips North America directly for guidance on next steps and potential remedies.
Yes, the gradient coil could overheat and cause smoke or fire, posing a risk of serious injury or property damage.
Check your system's model number and serial numbers against the list in the recall notice. Contact Philips North America for specific instructions.
Affected units have model number 781347 and specific serial numbers listed in the recall notice (e.g., 81001, 81003, etc.).
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2205-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2205-2025 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.
