Philips recalls Achieva XR MRI systems with specific model numbers due to potential fire risk from gradient coil component 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 Achieva XR MRI scanners because a component in the gradient coil could overheat and cause smoke or fire. This hazard requires immediate action to prevent potential fire risks.
The gradient coil component in the affected MRI systems can fail and act as a heat source, potentially producing smoke or fire. This risk occurs during normal operation and could lead to serious injury or property damage.
MRI system users and healthcare facilities that own or operate the recalled Achieva XR scanners with model numbers 781153 or 781253. Patients and staff are at risk if the scanner is used without addressing the issue.
Check your Achieva XR MRI scanner's model number. Affected units have model numbers 781153 or 781253. Serial numbers listed in the recall include specific ranges starting with 23003 and 35004.
Immediately stop using the affected Achieva XR MRI scanner if it has model numbers 781153 or 781253.
Model numbers 781153 and 781253 are affected.
Check your scanner's model number; affected units have model numbers 781153 or 781253. Serial numbers listed in the recall include specific ranges starting with 23003 and 35004.
Immediately stop using the scanner and contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2201-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2201-2025 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.
