Philips recalls Ingenia Elition X MRI scanners with specific model numbers (China only) due to potential fire from gradient coil failures. Affected units may produce smoke or fire.
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 Elition X MRI scanners sold in China because a component in the machine's gradient coil could overheat and cause smoke or fire. This is a serious hazard that requires immediate action.
The gradient coil in the affected MRI systems can fail and act as a heat source, potentially producing smoke or fire. This hazard occurs during normal operation and could lead to serious injury or property damage.
Owners of Ingenia Elition X MRI scanners with model numbers listed in the recall (China only) are affected. Medical facilities using these machines are at highest risk.
Check your scanner's model numbers: 781358, 782107, 782119, 782136, or 782151 (China only). Also verify the serial numbers listed in the recall notice.
Immediately stop using the affected MRI scanner if you own one with the listed model numbers in China.
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.
Model numbers 781358, 782107, 782119, 782136, and 782151 (China only).
The recall requires immediate stop use. Philips does not provide a repair or replacement option for this issue.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2211-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2211-2025 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.
