# Major Recall Alert: Philips MRI Systems (Achieva, Ingenia) Recalled Due to Risk of Smoke and Fire
Philips has issued an urgent recall of several MRI systems, including the **Achieva 3.0T MRI System - Main Unit**, **Ingenia 1.5T**, **Ingenia Ambition X**, and others. This decision comes after Philips identified serious safety concerns related to **component failures in the gradient coil**, which may act as a heat source with the potential to **produce smoke and/or fire**. Patients, operators, and even property are at risk due to possible **smoke inhalation, burns, and asphyxia**, which could result in injury or even death.
Read on to understand the critical details of this recall, the systems affected, and how you can protect yourself and your facility from further risk.
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## Why This Recall is Important
MRI machines play an essential role in diagnostics, but when a critical safety issue emerges, patient and operator safety take priority. The latest recall involves **gradient coil component failures** that may lead to severe safety hazards, including:
- **Repeated scan abort error messages** due to gradient amplifier faults.
- **Unusual noise** coming from the MRI system.
- A **burning smell**, which may escalate to visible smoke or fire.
The affected systems span across **gradient coil types WA15, WA30S, WB30S, and AG30S**, commonly used in major healthcare facilities. Beyond injuries, this issue could lead to **significant property damage** if fire-related incidents occur during operation. Immediate action is critical to mitigate risk.
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## Details of the Recall
### **Affected Models:**
Philips has identified several MRI systems within its recall notice, including:
- **Achieva 3.0T MRI System - Main Unit**
- **Achieva XR System - Main Unit**
- **Ingenia 1.5T**
- **Ingenia 3.0T**
- **Ingenia 3.0T CX**
- **Ingenia Ambition S**
- **Ingenia Ambition X**
- **Ingenia Elition X**
- **MR 7700**
### **Affected Gradient Coils:**
This safety issue pertains to MRI systems utilizing the gradient coil types:
- WA15
- WA30S
- WB30S
- AG30S
### **Recall Start Date:**
The recall has been in effect since **July 7, 2025**, with a primary aim to address these hazards before they escalate. If you operate one of these systems, immediate attention is essential. For more information, consult the [official recall notice](https://recalls-rappels.canada.ca/en/alert-recall/philips-achieva-and-ingenia-systems).
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## What You Should Do
If your facility uses one of the recalled systems, here are the recommended steps:
1. **Check Your MRI Systems**: Verify whether your machine is one of the affected models listed above.
2. **Monitor for Warning Signs**: Be alert for repeated scan abort errors, unusual noises, burning smells, smoke, or visible fire.
3. **Take Immediate Action**: If any of these symptoms appear, stop using the system and contact Philips support.
4. **Consult Philips**: Review their guidance on inspections, repairs, and replacements. This recall is a serious matter that should be addressed promptly to prevent harm.
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## Stay Safe – Get Instant Recall Alerts
Safety recalls like this emphasize the importance of staying informed about equipment used in healthcare settings. Missing a recall can have life-threatening consequences for patients and employees alike.
Stay proactive by downloading the **[MyRecalls App](https://myrecalls.app)** to receive **immediate alerts** about recalls for medical devices, equipment, and more. With this easy-to-use app, you can protect your staff, patients, and property by staying ahead of potential risks.
Don’t take chances—visit the [official recall page](https://recalls-rappels.canada.ca/en/alert-recall/philips-achieva-and-ingenia-systems) for complete details and download the app today!
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This recall highlights the importance of addressing equipment hazards without delay. Philips users should inspect their machinery promptly and consult experts to ensure safety. Protect your healthcare environment by staying informed—your awareness could save lives.